A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024613



Internal ID19113830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30646839..30738058hg38UCSC Ensembl
Innerchr9:30646837..30738056hg19UCSC Ensembl
Innerchr9:30636837..30728056hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3891220
hg1991220
hg1891220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7507n100
Supporting Variantsnssv3755923, nssv3755922
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024613
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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