A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522211



Internal ID15449504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:122103636..122191030hg38UCSC Ensembl
InnerchrX:121237489..121324883hg19UCSC Ensembl
InnerchrX:121065170..121152564hg18UCSC Ensembl
InnerchrX:120963024..121050418hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3887395
hg1987395
hg1887395
hg1787395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694987
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522211
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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