A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv727701



Internal ID16021657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161971429..162010712hg38UCSC Ensembl
Innerchr1:161941219..161980502hg19UCSC Ensembl
Innerchr1:160207843..160247126hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3839284
hg1939284
hg1839284
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548078
Supporting Variants
Samples
Known GenesOLFML2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv727701
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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