A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519165



Internal ID15099772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:48026897..48258328hg38UCSC Ensembl
InnerchrX:47886291..48117763hg19UCSC Ensembl
InnerchrX:47771235..48002707hg18UCSC Ensembl
InnerchrX:47642545..47874017hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38231432
hg19231473
hg18231473
hg17231473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696648
Samples
Known GenesSPACA5, SPACA5B, SSX1, SSX5, SSX6, ZNF630
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519165
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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