A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv736862



Internal ID16030818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:212824043..212836315hg38UCSC Ensembl
Innerchr1:212997385..213009657hg19UCSC Ensembl
Innerchr1:211064008..211076280hg18UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3812273
hg1912273
hg1812273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549149
Supporting Variants
Samples
Known GenesC1orf227
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv736862
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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