A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698361



Internal ID15088327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:15283411..15334052hg38UCSC Ensembl
InnerchrX:15301533..15352174hg19UCSC Ensembl
InnerchrX:15211454..15262095hg18UCSC Ensembl
InnerchrX:15061190..15111831hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3850642
hg1950642
hg1850642
hg1750642
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522729
Supporting Variants
Samples
Known GenesASB11, PIGA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698361
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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