A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13753907



Internal ID1619245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35887482..35889150hg38UCSC Ensembl
Innerchr10:35887518..35889115hg38UCSC Ensembl
Outerchr10:35887447..35889186hg38UCSC Ensembl
chr10:36176410..36178078hg19UCSC Ensembl
Innerchr10:36176446..36178043hg19UCSC Ensembl
Outerchr10:36176375..36178114hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg381669
hg191669
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622908
Supporting Variants
SamplesHG01500
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13753907
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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