A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690724



Internal ID18989005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22364574..22490687hg38UCSC Ensembl
Innerchr9:22364573..22490686hg19UCSC Ensembl
Innerchr9:22354573..22480686hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38126114
hg19126114
hg18126114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031822
Supporting Variants
Samples
Known GenesDMRTA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690724
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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