A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3688828



Internal ID18987109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30426107..30563356hg38UCSC Ensembl
Innerchr9:30426105..30563354hg19UCSC Ensembl
Innerchr9:30416105..30553354hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38137250
hg19137250
hg18137250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025249
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3688828
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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