A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13950770



Internal ID3952586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120726759..121011020hg38UCSC Ensembl
chr10:122486271..122770533hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38284262
hg19284263
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624737
Supporting Variants
SamplesHG02144
Known GenesMIR5694, WDR11, WDR11-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13950770
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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