A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613705



Internal ID16401114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17699983..17726583hg38UCSC Ensembl
Innerchr9:17699981..17726581hg19UCSC Ensembl
Innerchr9:17689981..17716581hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3826601
hg1926601
hg1826601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156263
SamplesHGDP00602
Known GenesSH3GL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613705
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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