A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516791



Internal ID15444084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:106805618..106810920hg38UCSC Ensembl
Innerchr8:107817846..107823148hg19UCSC Ensembl
Innerchr8:107887022..107892324hg18UCSC Ensembl
Innerchr8:107887022..107892324hg17UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg385303
hg195303
hg185303
hg175303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv468n21
Supporting Variantsnssv679481, nssv691762, nssv670897, nssv663330, nssv681678, nssv691300, nssv679134
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516791
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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