A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13861553



Internal ID4443629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72052724..72055085hg38UCSC Ensembl
Innerchr10:72052732..72055078hg38UCSC Ensembl
Outerchr10:72052717..72055093hg38UCSC Ensembl
chr10:73812482..73814843hg19UCSC Ensembl
Innerchr10:73812490..73814836hg19UCSC Ensembl
Outerchr10:73812475..73814851hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382362
hg192362
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623789
Supporting Variants
SamplesHG03950
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13861553
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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