A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv734980



Internal ID15682250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:206011786..206014870hg38UCSC Ensembl
Innerchr1:206326498..206329582hg19UCSC Ensembl
Innerchr1:204493121..204496205hg18UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg383085
hg193085
hg183085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549066
Supporting Variants
Samples
Known GenesCTSE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv734980
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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