A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698542



Internal ID15435194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:47978461..48062292hg38UCSC Ensembl
InnerchrX:47837860..47921671hg19UCSC Ensembl
InnerchrX:47722804..47806615hg18UCSC Ensembl
InnerchrX:47594114..47677925hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3883832
hg1983812
hg1883812
hg1783812
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522886
Supporting Variants
Samples
Known GenesSPACA5, SPACA5B, ZNF182, ZNF630
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698542
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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