A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042238



Internal ID19131457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:80304115..80461286hg38UCSC Ensembl
Innerchr9:82919030..83076201hg19UCSC Ensembl
Innerchr9:82108850..82266021hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38157172
hg19157172
hg18157172
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7685n100
Supporting Variantsnssv3697516, nssv3697515
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)nsv1042238
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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