A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521626



Internal ID15448919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:78317599..78415846hg38UCSC Ensembl
Innerchr9:80932515..81030762hg19UCSC Ensembl
Innerchr9:80122335..80220582hg18UCSC Ensembl
Innerchr9:78162069..78260316hg17UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3898248
hg1998248
hg1898248
hg1798248
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698245
Samples
Known GenesPSAT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521626
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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