A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528121



Internal ID15455414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:95206606..95212001hg38UCSC Ensembl
Innerchr14:95672943..95678338hg19UCSC Ensembl
Innerchr14:94742696..94748091hg18UCSC Ensembl
Innerchr14:94742696..94748091hg17UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg385396
hg195396
hg185396
hg175396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704664
Samples
Known GenesCLMN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528121
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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