A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519486



Internal ID15446779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:45266258..45401909hg38UCSC Ensembl
InnerchrX:45125503..45261154hg19UCSC Ensembl
InnerchrX:45010447..45146098hg18UCSC Ensembl
InnerchrX:44881757..45017408hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38135652
hg19135652
hg18135652
hg17135652
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv685137, nssv656380, nssv681812, nssv699234, nssv685890, nssv695715
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519486
Frequency
Sample Size2026
Observed Gain5
Observed Loss1
Observed Complex0
Frequencyn/a


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