A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698245



Internal ID15434897
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521626
Supporting Variants
Samples
Known GenesPSAT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698245
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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