A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13756704



Internal ID3797600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36910733..37042861hg38UCSC Ensembl
chr10:37199661..37331789hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38132129
hg19132129
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622940
Supporting Variants
SamplesHG03445
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13756704
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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