A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13963704



Internal ID579486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125332986..125340008hg38UCSC Ensembl
Innerchr10:125332992..125340003hg38UCSC Ensembl
Outerchr10:125332981..125340014hg38UCSC Ensembl
chr10:127021555..127028577hg19UCSC Ensembl
Innerchr10:127021561..127028572hg19UCSC Ensembl
Outerchr10:127021550..127028583hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg387023
hg197023
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624830
Supporting Variants
SamplesHG00254
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13963704
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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