A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13964546



Internal ID5389783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126259122..126270242hg38UCSC Ensembl
chr10:127947691..127958811hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3811121
hg1911121
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624853
Supporting Variants
SamplesNA18939
Known GenesADAM12
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13964546
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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