A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516771



Internal ID15097378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:107155014..107160257hg38UCSC Ensembl
Innerchr6:107476218..107481461hg19UCSC Ensembl
Innerchr6:107582911..107588154hg18UCSC Ensembl
Innerchr6:107582911..107588154hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385244
hg195244
hg185244
hg175244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv670741, nssv660417, nssv692857
Samples
Known GenesPDSS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516771
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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