A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519509



Internal ID15446802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:126759578..127239638hg38UCSC Ensembl
InnerchrX:125893561..126373621hg19UCSC Ensembl
InnerchrX:125721242..126201302hg18UCSC Ensembl
InnerchrX:125619096..126099156hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38480061
hg19480061
hg18480061
hg17480061
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv661583, nssv678627, nssv683849, nssv704399, nssv682123, nssv656454, nssv703689, nssv690334, nssv692288, nssv682124, nssv683848, nssv659121
Samples
Known GenesCXorf64
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519509
Frequency
Sample Size2026
Observed Gain8
Observed Loss4
Observed Complex0
Frequencyn/a


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