A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697798



Internal ID15087764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:107068757..107081142hg38UCSC Ensembl
InnerchrX:106311987..106324372hg19UCSC Ensembl
InnerchrX:106198643..106211028hg18UCSC Ensembl
InnerchrX:106118132..106130517hg17UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3812386
hg1912386
hg1812386
hg1712386
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519484
Supporting Variants
Samples
Known GenesRBM41
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697798
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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