A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696321



Internal ID15086287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:107065186..107153172hg38UCSC Ensembl
InnerchrX:106308416..106396402hg19UCSC Ensembl
InnerchrX:106195072..106283058hg18UCSC Ensembl
InnerchrX:106114561..106202547hg17UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3887987
hg1987987
hg1887987
hg1787987
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519484
Supporting Variants
Samples
Known GenesNUP62CL, RBM41
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696321
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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