A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690767



Internal ID15080733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:12768002..12803775hg38UCSC Ensembl
InnerchrX:12786121..12821894hg19UCSC Ensembl
InnerchrX:12696042..12731815hg18UCSC Ensembl
InnerchrX:12545778..12581551hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3835774
hg1935774
hg1835774
hg1735774
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520250
Supporting Variants
Samples
Known GenesPRPS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690767
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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