A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698061



Internal ID15088027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:39655232..39823739hg38UCSC Ensembl
InnerchrX:39514486..39682993hg19UCSC Ensembl
InnerchrX:39399430..39567937hg18UCSC Ensembl
InnerchrX:39270702..39439217hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38168508
hg19168508
hg18168508
hg17168516
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521450
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698061
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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