A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524356



Internal ID15451649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:127503869..127564723hg38UCSC Ensembl
InnerchrX:126637850..126698704hg19UCSC Ensembl
InnerchrX:126465531..126526385hg18UCSC Ensembl
InnerchrX:126363385..126424239hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3860855
hg1960855
hg1860855
hg1760855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv530n21
Supporting Variantsnssv700265
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524356
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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