A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041876



Internal ID19131095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125992377..126025209hg38UCSC Ensembl
Innerchr9:128754656..128787488hg19UCSC Ensembl
Innerchr9:127794477..127827309hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3832833
hg1932833
hg1832833
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7715n100
Supporting Variantsnssv3695235, nssv3695236
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)nsv1041876
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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