A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015810



Internal ID19105028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17590301..17633298hg38UCSC Ensembl
Innerchr9:17590299..17633296hg19UCSC Ensembl
Innerchr9:17580299..17623296hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3842998
hg1942998
hg1842998
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7466n100
Supporting Variantsnssv3690664, nssv3755824
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)nsv1015810
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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