A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526412



Internal ID15453705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:87210687..87747441hg38UCSC Ensembl
InnerchrX:86465690..87002441hg19UCSC Ensembl
InnerchrX:86352346..86889097hg18UCSC Ensembl
InnerchrX:86271835..86808586hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38536755
hg19536752
hg18536752
hg17536752
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702712
Samples
Known GenesKLHL4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526412
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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