A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028155



Internal ID19117373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20005038..20029284hg38UCSC Ensembl
Innerchr9:20005036..20029282hg19UCSC Ensembl
Innerchr9:19995036..20019282hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3824247
hg1924247
hg1824247
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755830
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)nsv1028155
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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