A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705837



Internal ID15442489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:146388801..146423929hg38UCSC Ensembl
InnerchrX:145470319..145505447hg19UCSC Ensembl
InnerchrX:145278011..145313139hg18UCSC Ensembl
InnerchrX:145175865..145210993hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3835129
hg1935129
hg1835129
hg1735129
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517790
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705837
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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