A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015149



Internal ID19104366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:1722601..1759811hg38UCSC Ensembl
Innerchr9:1722601..1759811hg19UCSC Ensembl
Innerchr9:1712601..1749811hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3837211
hg1937211
hg1837211
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7375n100
Supporting Variantsnssv3758081
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)nsv1015149
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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