A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698353



Internal ID15435005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:137095116..137167548hg38UCSC Ensembl
InnerchrX:136177275..136249707hg19UCSC Ensembl
InnerchrX:136004941..136077373hg18UCSC Ensembl
InnerchrX:135902795..135975227hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3872433
hg1972433
hg1872433
hg1772433
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522722
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698353
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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