A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031822



Internal ID19121044
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 StatusM
Merged Variants
Supporting Variantsnssv3690724
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)nsv1031822
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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