A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv734945



Internal ID15682215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:206113879..206117999hg38UCSC Ensembl
Innerchr1:206223332..206227452hg19UCSC Ensembl
Innerchr1:204389955..204394075hg18UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg384121
hg194121
hg184121
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549046
Supporting Variants
Samples
Known GenesAVPR1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv734945
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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