A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034049



Internal ID19123271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19954350..20049822hg38UCSC Ensembl
Innerchr9:19954348..20049820hg19UCSC Ensembl
Innerchr9:19944348..20039820hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3895473
hg1995473
hg1895473
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690693
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)nsv1034049
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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