A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3755890



Internal ID19054171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28588577..28768828hg38UCSC Ensembl
Innerchr9:28588575..28768826hg19UCSC Ensembl
Innerchr9:28578575..28758826hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38180252
hg19180252
hg18180252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028793
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)nssv3755890
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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