A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673217



Internal ID15409869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:48032343..48108258hg38UCSC Ensembl
InnerchrX:47891738..47967642hg19UCSC Ensembl
InnerchrX:47776682..47852586hg18UCSC Ensembl
InnerchrX:47647992..47723896hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3875916
hg1975905
hg1875905
hg1775905
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517350
Supporting Variants
Samples
Known GenesSSX6, ZNF630
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673217
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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