A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549934



Internal ID16337343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:7620489..7636664hg38UCSC Ensembl
Innerchr10:7662452..7678627hg19UCSC Ensembl
Innerchr10:7702458..7718633hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3816176
hg1916176
hg1816176
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv743968
Samples
Known GenesITIH5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549934
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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