A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018926



Internal ID18761459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:965006..1014141hg38UCSC Ensembl
Innerchr9:965006..1014141hg19UCSC Ensembl
Innerchr9:955006..1004141hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3849136
hg1949136
hg1849136
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7371n100
Supporting Variantsnssv3691210
Samples
Known GenesDMRT1, DMRT3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018926
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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