A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034673



Internal ID18777206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17739008..17916608hg38UCSC Ensembl
Innerchr9:17739006..17916606hg19UCSC Ensembl
Innerchr9:17729006..17906606hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38177601
hg19177601
hg18177601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7468n100
Supporting Variantsnssv3690670
Samples
Known GenesSH3GL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034673
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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