A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13974231



Internal ID4647744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129796909..129797209hg38UCSC Ensembl
Innerchr10:129796909..129797209hg38UCSC Ensembl
Outerchr10:129796909..129797209hg38UCSC Ensembl
chr10:131595173..131595473hg19UCSC Ensembl
Innerchr10:131595173..131595473hg19UCSC Ensembl
Outerchr10:131595173..131595473hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624924
Supporting Variants
SamplesHG04177
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13974231
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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