A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv736893



Internal ID16030849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:212830086..212834885hg38UCSC Ensembl
Innerchr1:213003428..213008227hg19UCSC Ensembl
Innerchr1:211070051..211074850hg18UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg384800
hg194800
hg184800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549159
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)nssv736893
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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