A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156737



Internal ID15880104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25562456..25598676hg38UCSC Ensembl
Innerchr9:25562454..25598674hg19UCSC Ensembl
Innerchr9:25552454..25588674hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3836221
hg1936221
hg1836221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613914
Supporting Variants
SamplesNINDS_156
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156737
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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