A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694599



Internal ID15431251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5669572..5679293hg38UCSC Ensembl
InnerchrX:5587613..5597334hg19UCSC Ensembl
InnerchrX:5597613..5607334hg18UCSC Ensembl
InnerchrX:5447349..5457070hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg389722
hg199722
hg189722
hg179722
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521826
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694599
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer