A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522897



Internal ID15450190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:145220452..145273019hg38UCSC Ensembl
InnerchrX:144301972..144354539hg19UCSC Ensembl
InnerchrX:144109664..144162231hg18UCSC Ensembl
InnerchrX:144007518..144060085hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3852568
hg1952568
hg1852568
hg1752568
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698555
Samples
Known GenesSPANXN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522897
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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