A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690671



Internal ID18642266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17748813..17919576hg38UCSC Ensembl
Innerchr9:17748811..17919574hg19UCSC Ensembl
Innerchr9:17738811..17909574hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38170764
hg19170764
hg18170764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023089
Supporting Variants
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)nssv3690671
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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