A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032604



Internal ID19121826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17585689..17633298hg38UCSC Ensembl
Innerchr9:17585687..17633296hg19UCSC Ensembl
Innerchr9:17575687..17623296hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3847610
hg1947610
hg1847610
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7466n100
Supporting Variantsnssv3755821, nssv3690654, nssv3690653, nssv3755819, nssv3690655, nssv3755818, nssv3755816, nssv3755817, nssv3755822, nssv3755820, nssv3690656
Samples
Known GenesSH3GL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032604
Frequency
Sample Size11257
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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