A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703547



Internal ID15440199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:118502516..118593364hg38UCSC Ensembl
InnerchrX:117636479..117727327hg19UCSC Ensembl
InnerchrX:117520507..117611355hg18UCSC Ensembl
InnerchrX:117418361..117509209hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3890849
hg1990849
hg1890849
hg1790849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517257
Supporting Variants
Samples
Known GenesDOCK11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703547
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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