A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696648



Internal ID15086614
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519165
Supporting Variants
Samples
Known GenesSPACA5, SPACA5B, SSX1, SSX5, SSX6, ZNF630
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696648
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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