A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv712409



Internal ID16006365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:38588885..38619564hg38UCSC Ensembl
Innerchr1:39054557..39085236hg19UCSC Ensembl
Innerchr1:38827144..38857823hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3830680
hg1930680
hg1830680
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546034
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv712409
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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