A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638268



Internal ID7025054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25104030..25105498hg38UCSC Ensembl
Innerchr16:25104059..25105470hg38UCSC Ensembl
Outerchr16:25104002..25105527hg38UCSC Ensembl
chr16:25115351..25116819hg19UCSC Ensembl
Innerchr16:25115380..25116791hg19UCSC Ensembl
Outerchr16:25115323..25116848hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381469
hg191469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15431192, essv15431196, essv15431194, essv15431191, essv15431187, essv15431190, essv15431188, essv15431195, essv15431186, essv15431185, essv15431193, essv15431189
SamplesHG02811, HG03135, HG02756, NA19901, NA19200, HG02757, NA18856, HG02675, NA19117, NA19713, HG02768, NA19096
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638268
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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