A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156260



Internal ID15880372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17583312..17631554hg38UCSC Ensembl
Innerchr9:17583310..17631552hg19UCSC Ensembl
Innerchr9:17573310..17621552hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3848243
hg1948243
hg1848243
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613703
Supporting Variants
SamplesNINDS_200
Known GenesSH3GL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156260
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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