A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516020



Internal ID15443077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:12157437..12182323hg38UCSC Ensembl
Innerchr17:12060754..12085640hg19UCSC Ensembl
Innerchr17:12001479..12026365hg18UCSC Ensembl
Innerchr17:12001479..12026365hg17UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3824887
hg1924887
hg1824887
hg1724887
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv177n21
Supporting Variantsnssv683742, nssv672525, nssv657043, nssv665765
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516020
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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