A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517679



Internal ID15444972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:98582884..98673534hg38UCSC Ensembl
InnerchrX:97837882..97928532hg19UCSC Ensembl
InnerchrX:97724538..97815188hg18UCSC Ensembl
InnerchrX:97644027..97734677hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3890651
hg1990651
hg1890651
hg1790651
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv521n21
Supporting Variantsnssv661865, nssv690710, nssv678903, nssv652812, nssv670900, nssv688512
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517679
Frequency
Sample Size2026
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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