A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696889



Internal ID15433541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:153974269..153982503hg38UCSC Ensembl
InnerchrX:153239720..153247954hg19UCSC Ensembl
InnerchrX:152892914..152901148hg18UCSC Ensembl
InnerchrX:152760567..152768801hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg388235
hg198235
hg188235
hg178235
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519506
Supporting Variants
Samples
Known GenesMIR3202-1, MIR3202-2, TMEM187
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696889
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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