A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698360



Internal ID15088326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:101596330..101656080hg38UCSC Ensembl
InnerchrX:100851308..100911066hg19UCSC Ensembl
InnerchrX:100737964..100797722hg18UCSC Ensembl
InnerchrX:100657453..100717211hg17UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3859751
hg1959759
hg1859759
hg1759759
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522728
Supporting Variants
Samples
Known GenesARMCX2, ARMCX3, ARMCX6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698360
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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