A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545991



Internal ID16333400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:34802236..34813575hg38UCSC Ensembl
Innerchr1:35267837..35279176hg19UCSC Ensembl
Innerchr1:35040424..35051763hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3811340
hg1911340
hg1811340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv712317, nssv712316, nssv712318, nssv712315, nssv712313, nssv712314
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545991
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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