A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681135



Internal ID15071101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18996430..18999580hg38UCSC Ensembl
Innerchr8:18853940..18857090hg19UCSC Ensembl
Innerchr8:18898220..18901370hg18UCSC Ensembl
Innerchr8:18898220..18901370hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg383151
hg193151
hg183151
hg173151
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517395
Supporting Variants
Samples
Known GenesPSD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681135
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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