A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670446



Internal ID15407098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:70718230..70809262hg38UCSC Ensembl
InnerchrX:69938080..70029112hg19UCSC Ensembl
InnerchrX:69854805..69945837hg18UCSC Ensembl
InnerchrX:69721101..69812133hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3891033
hg1991033
hg1891033
hg1791033
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517078
Supporting Variants
Samples
Known GenesTEX11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670446
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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