A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3688855



Internal ID18987136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31560620..31603347hg38UCSC Ensembl
Innerchr9:31560618..31603345hg19UCSC Ensembl
Innerchr9:31550618..31593345hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3842728
hg1942728
hg1842728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024541
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)nssv3688855
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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