A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523595



Internal ID15104202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:48204340..48359634hg38UCSC Ensembl
InnerchrX:48063776..48219069hg19UCSC Ensembl
InnerchrX:47948720..48104013hg18UCSC Ensembl
InnerchrX:47820030..47975323hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38155295
hg19155294
hg18155294
hg17155294
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699387
Samples
Known GenesSSX1, SSX3, SSX9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523595
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