A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700342



Internal ID15436994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5536476..5567466hg38UCSC Ensembl
InnerchrX:5454517..5485507hg19UCSC Ensembl
InnerchrX:5464517..5495507hg18UCSC Ensembl
InnerchrX:5314253..5345243hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3830991
hg1930991
hg1830991
hg1730991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524416
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700342
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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