A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528176



Internal ID15108783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:89305771..89309840hg38UCSC Ensembl
Innerchr14:89772115..89776184hg19UCSC Ensembl
Innerchr14:88841868..88845937hg18UCSC Ensembl
Innerchr14:88841868..88845937hg17UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg384070
hg194070
hg184070
hg174070
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704726
Samples
Known GenesFOXN3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528176
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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