A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3755892



Internal ID19054173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28592529..28761733hg38UCSC Ensembl
Innerchr9:28592527..28761731hg19UCSC Ensembl
Innerchr9:28582527..28751731hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38169205
hg19169205
hg18169205
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032891
Supporting Variants
Samples
Known GenesLINGO2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3755892
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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