A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523353



Internal ID15450646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:121396133..121508293hg38UCSC Ensembl
InnerchrX:120529987..120642147hg19UCSC Ensembl
InnerchrX:120357668..120469828hg18UCSC Ensembl
InnerchrX:120255522..120367682hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38112161
hg19112161
hg18112161
hg17112161
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv528n21
Supporting Variantsnssv699102
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523353
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