A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13738678



Internal ID2393261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28770635..28776133hg38UCSC Ensembl
Innerchr10:28770656..28776112hg38UCSC Ensembl
Outerchr10:28770614..28776154hg38UCSC Ensembl
chr10:29059564..29065062hg19UCSC Ensembl
Innerchr10:29059585..29065041hg19UCSC Ensembl
Outerchr10:29059543..29065083hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg385499
hg195499
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622755
Supporting Variants
SamplesHG02122
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13738678
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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