A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516732



Internal ID15444025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:133374094..133382034hg38UCSC Ensembl
Innerchr8:134386337..134394277hg19UCSC Ensembl
Innerchr8:134455519..134463459hg18UCSC Ensembl
Innerchr8:134455519..134463459hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg387941
hg197941
hg187941
hg177941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv655374, nssv670499, nssv692015
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516732
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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