A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528343



Internal ID15108950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:15271931..15385229hg38UCSC Ensembl
InnerchrX:15290053..15403351hg19UCSC Ensembl
InnerchrX:15199974..15313272hg18UCSC Ensembl
InnerchrX:15049710..15163008hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38113299
hg19113299
hg18113299
hg17113299
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704925
Samples
Known GenesASB11, FIGF, PIGA, PIR, PIR-FIGF
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528343
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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