A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516738



Internal ID15444031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:114864258..114886242hg38UCSC Ensembl
Innerchr6:115185422..115207406hg19UCSC Ensembl
Innerchr6:115292115..115314099hg18UCSC Ensembl
Innerchr6:115292115..115314099hg17UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3821985
hg1921985
hg1821985
hg1721985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv689616, nssv677989, nssv670544
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516738
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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