A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528258



Internal ID15108865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:91049415..92236799hg38UCSC Ensembl
InnerchrX:90304414..91491798hg19UCSC Ensembl
InnerchrX:90191070..91378454hg18UCSC Ensembl
InnerchrX:90110559..91297943hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg381187385
hg191187385
hg181187385
hg171187385
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704824
Samples
Known GenesPABPC5, PCDH11X
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528258
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