A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698833



Internal ID15088799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:130937509..131062354hg38UCSC Ensembl
InnerchrX:130071483..130196328hg19UCSC Ensembl
InnerchrX:129899164..130024009hg18UCSC Ensembl
InnerchrX:129797018..129921863hg17UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg38124846
hg19124846
hg18124846
hg17124846
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523130
Supporting Variants
Samples
Known GenesARHGAP36
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698833
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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