A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691213



Internal ID18642808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:1003311..1124524hg38UCSC Ensembl
Innerchr9:1003311..1124524hg19UCSC Ensembl
Innerchr9:993311..1114524hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38121214
hg19121214
hg18121214
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025752
Supporting Variants
Samples
Known GenesDMRT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3691213
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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