A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702264



Internal ID15092230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:20149203..20206450hg38UCSC Ensembl
InnerchrX:20167321..20224568hg19UCSC Ensembl
InnerchrX:20077242..20134489hg18UCSC Ensembl
InnerchrX:19926978..19984225hg17UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3857248
hg1957248
hg1857248
hg1757248
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526033
Supporting Variants
Samples
Known GenesRPS6KA3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702264
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