A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702616



Internal ID15092582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:89193216..89194643hg38UCSC Ensembl
Innerchr14:89659560..89660987hg19UCSC Ensembl
Innerchr14:88729313..88730740hg18UCSC Ensembl
Innerchr14:88729313..88730740hg17UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg381428
hg191428
hg181428
hg171428
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526326
Supporting Variants
Samples
Known GenesFOXN3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702616
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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