A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3755948



Internal ID19054229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39455352..39747836hg38UCSC Ensembl
Innerchr9:41600370..41892854hg19UCSC Ensembl
Innerchr9:41590370..41882854hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38292485
hg19292485
hg18292485
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033156
Supporting Variants
Samples
Known GenesLOC653501
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3755948
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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