A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14082595



Internal ID21285536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:44410690..44413973hg38UCSC Ensembl
Innerchr5:44410792..44414075hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg383284
hg193284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112401
Supporting Variants
Samplessample375
Known GenesFGF10-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14082595
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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