A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv736916



Internal ID16030872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:212830086..212844783hg38UCSC Ensembl
Innerchr1:213003428..213018125hg19UCSC Ensembl
Innerchr1:211070051..211084748hg18UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3814698
hg1914698
hg1814698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549163
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)nssv736916
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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