A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176152



Internal ID15881310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129384126..129405288hg38UCSC Ensembl
Innerchr9:132146405..132167567hg19UCSC Ensembl
Innerchr9:131186226..131207388hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3821163
hg1921163
hg1821163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615427
Supporting Variants
SamplesNINDS_98
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176152
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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