A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700825



Internal ID15437477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:115046174..115048882hg38UCSC Ensembl
InnerchrX:114280737..114283445hg19UCSC Ensembl
InnerchrX:114186993..114189701hg18UCSC Ensembl
InnerchrX:114103717..114106425hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg382709
hg192709
hg182709
hg172709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516624
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700825
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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