A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517789



Internal ID15445082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:131100726..131206649hg38UCSC Ensembl
InnerchrX:130234700..130340623hg19UCSC Ensembl
InnerchrX:130062381..130168304hg18UCSC Ensembl
InnerchrX:129960235..130066158hg17UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg38105924
hg19105924
hg18105924
hg17105924
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv653271, nssv694597, nssv682565
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517789
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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