A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613703



Internal ID16401112
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 StatusM
Merged Variantsdgv12581n54
Supporting Variantsnssv1129331, nssv1156260
SamplesNINDS_200
Known GenesSH3GL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613703
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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