A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516516



Internal ID15097123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85525117..85568973hg38UCSC Ensembl
Innerchr6:86234835..86278691hg19UCSC Ensembl
Innerchr6:86291554..86335410hg18UCSC Ensembl
Innerchr6:86291554..86335410hg17UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3843857
hg1943857
hg1843857
hg1743857
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv679849, nssv699272, nssv687806, nssv678496, nssv684014, nssv669782, nssv668794, nssv677138
Samples
Known GenesSNX14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516516
Frequency
Sample Size2026
Observed Gain1
Observed Loss7
Observed Complex0
Frequencyn/a


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