A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156454



Internal ID15856044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21037772..21082815hg38UCSC Ensembl
Innerchr9:21037771..21082814hg19UCSC Ensembl
Innerchr9:21027771..21072814hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3845044
hg1945044
hg1845044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613753
Supporting Variants
Samples1798860565_A
Known GenesIFNB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156454
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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