A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528614



Internal ID15109221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26893664..27074235hg38UCSC Ensembl
Innerchr9:26893662..27074233hg19UCSC Ensembl
Innerchr9:26883662..27064233hg18UCSC Ensembl
Innerchr9:26883662..27064233hg17UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38180572
hg19180572
hg18180572
hg17180572
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705242
Samples
Known GenesIFT74, LRRC19, PLAA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528614
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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