A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659811



Internal ID15049777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143933019..143972494hg38UCSC Ensembl
Innerchr8:145007187..145046662hg19UCSC Ensembl
Innerchr8:145079175..145118650hg18UCSC Ensembl
Innerchr8:145079175..145118650hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3839476
hg1939476
hg1839476
hg1739476
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515809
Supporting Variants
Samples
Known GenesMIR661, PLEC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659811
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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