A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624423



Internal ID7011278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103956027..103960936hg38UCSC Ensembl
Innerchr10:103956054..103960910hg38UCSC Ensembl
Outerchr10:103956001..103960963hg38UCSC Ensembl
chr10:105715785..105720694hg19UCSC Ensembl
Innerchr10:105715812..105720668hg19UCSC Ensembl
Outerchr10:105715759..105720721hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg384910
hg194910
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13915172, essv13915166, essv13915185, essv13915184, essv13915182, essv13915177, essv13915170, essv13915171, essv13915156, essv13915163, essv13915154, essv13915187, essv13915174, essv13915188, essv13915161, essv13915158, essv13915168, essv13915176, essv13915183, essv13915178, essv13915157, essv13915169, essv13915164, essv13915179, essv13915181, essv13915180, essv13915165, essv13915159, essv13915175, essv13915173, essv13915155, essv13915186, essv13915160, essv13915162, essv13915167
SamplesNA19058, HG01356, HG01965, HG01326, HG01389, NA18999, HG01924, HG01250, NA19746, HG01953, HG02105, HG01997, NA19723, NA19649, HG02299, HG01372, HG01973, HG01932, HG02104, HG01565, HG01435, NA19086, HG01938, NA19658, HG01149, HG01311, HG02008, HG01921, HG02292, HG01992, HG01939, HG01977, HG01556, HG02348, HG01566
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624423
Frequency
Sample Size2504
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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