A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527680



Internal ID15454973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:145250160..145384001hg38UCSC Ensembl
InnerchrX:144331680..144465519hg19UCSC Ensembl
InnerchrX:144139372..144273211hg18UCSC Ensembl
InnerchrX:144037226..144171065hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38133842
hg19133840
hg18133840
hg17133840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv537n21
Supporting Variantsnssv704155
Samples
Known GenesSPANXN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527680
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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