A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517339



Internal ID15097946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77270169..77283227hg38UCSC Ensembl
Innerchr17:75266251..75279309hg19UCSC Ensembl
Innerchr17:72777846..72790904hg18UCSC Ensembl
Innerchr17:72777846..72790904hg17UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3813059
hg1913059
hg1813059
hg1713059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv680553, nssv676147, nssv683433, nssv678375, nssv671000, nssv651774, nssv682199
Samples
Known GenesSEPT9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517339
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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