A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963095



Internal ID15910365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52820319..52826790hg38UCSC Ensembl
Innerchr3:52854335..52860806hg19UCSC Ensembl
Innerchr3:52829375..52835846hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg386472
hg196472
hg186472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590308
Supporting Variants
Samples
Known GenesITIH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv963095
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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