A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517783



Internal ID15445076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:860832..875010hg38UCSC Ensembl
Innerchr17:764072..778250hg19UCSC Ensembl
Innerchr17:710822..725000hg18UCSC Ensembl
Innerchr17:710822..725000hg17UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3814179
hg1914179
hg1814179
hg1714179
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv682324, nssv667568, nssv653240
Samples
Known GenesNXN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517783
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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