A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697385



Internal ID15434037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:111916179..111943013hg38UCSC Ensembl
InnerchrX:111159407..111186241hg19UCSC Ensembl
InnerchrX:111046063..111072897hg18UCSC Ensembl
InnerchrX:110965552..110992386hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3826835
hg1926835
hg1826835
hg1726835
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520386
Supporting Variants
Samples
Known GenesTRPC5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697385
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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