A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13964285



Internal ID6591786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125617667..125702765hg38UCSC Ensembl
Innerchr10:125617667..125702765hg38UCSC Ensembl
Outerchr10:125617167..125703265hg38UCSC Ensembl
chr10:127306236..127391334hg19UCSC Ensembl
Innerchr10:127306236..127391334hg19UCSC Ensembl
Outerchr10:127305736..127391834hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3885099
hg1985099
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624839
Supporting Variants
SamplesNA20768
Known GenesLOC283038, TEX36
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13964285
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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