A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021193



Internal ID18763727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:978833..1020933hg38UCSC Ensembl
Innerchr9:978833..1020933hg19UCSC Ensembl
Innerchr9:968833..1010933hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3842101
hg1942101
hg1842101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7371n100
Supporting Variantsnssv3691211, nssv3691212
Samples
Known GenesDMRT3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021193
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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