A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683425



Internal ID15073391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:15388939..15397461hg38UCSC Ensembl
InnerchrX:15407061..15415583hg19UCSC Ensembl
InnerchrX:15316982..15325504hg18UCSC Ensembl
InnerchrX:15166718..15175240hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg388523
hg198523
hg188523
hg178523
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515969
Supporting Variants
Samples
Known GenesPIR, PIR-FIGF
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683425
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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