A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699574



Internal ID15436226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:35091453..35130905hg38UCSC Ensembl
InnerchrX:35109570..35149022hg19UCSC Ensembl
InnerchrX:35019491..35058943hg18UCSC Ensembl
InnerchrX:34869227..34908679hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3839453
hg1939453
hg1839453
hg1739453
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523756
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699574
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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