A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697431



Internal ID15087397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:101007183..101038566hg38UCSC Ensembl
InnerchrX:100262172..100293555hg19UCSC Ensembl
InnerchrX:100148828..100180211hg18UCSC Ensembl
InnerchrX:100068317..100099700hg17UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3831384
hg1931384
hg1831384
hg1731384
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515758
Supporting Variants
Samples
Known GenesTRMT2B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697431
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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