A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024816



Internal ID19114033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31590397..31658695hg38UCSC Ensembl
Innerchr9:31590395..31658693hg19UCSC Ensembl
Innerchr9:31580395..31648693hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3868299
hg1968299
hg1868299
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688858, nssv3688857
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)nsv1024816
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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