A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13757115



Internal ID3758931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37789403..37797452hg38UCSC Ensembl
Innerchr10:37789403..37797452hg38UCSC Ensembl
Outerchr10:37789297..37797601hg38UCSC Ensembl
chr10:38078331..38086380hg19UCSC Ensembl
Innerchr10:38078331..38086380hg19UCSC Ensembl
Outerchr10:38078225..38086529hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg388050
hg198050
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622970
Supporting Variants
SamplesHG03854
Known GenesZNF248, ZNF33BP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13757115
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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