A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv728815



Internal ID15676085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:171339693..171402859hg38UCSC Ensembl
Innerchr1:171308832..171371998hg19UCSC Ensembl
Innerchr1:169575456..169638622hg18UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg3863167
hg1963167
hg1863167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548188
Supporting Variants
Samples
Known GenesFMO4, TOP1P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv728815
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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