A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624492



Internal ID7011345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:107862552..107941308hg38UCSC Ensembl
Innerchr10:107862555..107941305hg38UCSC Ensembl
Outerchr10:107862549..107941311hg38UCSC Ensembl
chr10:109622310..109701066hg19UCSC Ensembl
Innerchr10:109622313..109701063hg19UCSC Ensembl
Outerchr10:109622307..109701069hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3878757
hg1978757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13932803
SamplesHG00620
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624492
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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