A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700696



Internal ID15090662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:101596330..101625867hg38UCSC Ensembl
InnerchrX:100851308..100880857hg19UCSC Ensembl
InnerchrX:100737964..100767513hg18UCSC Ensembl
InnerchrX:100657453..100687002hg17UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3829538
hg1929550
hg1829550
hg1729550
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524711
Supporting Variants
Samples
Known GenesARMCX3, ARMCX6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700696
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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