A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527777



Internal ID15455070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:126752721..126781502hg38UCSC Ensembl
InnerchrX:125886704..125915485hg19UCSC Ensembl
InnerchrX:125714385..125743166hg18UCSC Ensembl
InnerchrX:125612239..125641020hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3828782
hg1928782
hg1828782
hg1728782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704268
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527777
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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