A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519637



Internal ID15446930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:116658885..116708191hg38UCSC Ensembl
InnerchrX:115792853..115842159hg19UCSC Ensembl
InnerchrX:115676881..115726187hg18UCSC Ensembl
InnerchrX:115574735..115624041hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3849307
hg1949307
hg1849307
hg1749307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv659648, nssv657311, nssv658005
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519637
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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