A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686519



Internal ID15423171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:70664728..70720583hg38UCSC Ensembl
InnerchrX:69884578..69940433hg19UCSC Ensembl
InnerchrX:69801303..69857158hg18UCSC Ensembl
InnerchrX:69667599..69723454hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3855856
hg1955856
hg1855856
hg1755856
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)nssv686519
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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