A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096630



Internal ID21269200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:37513373..37515797hg38UCSC Ensembl
Innerchr1:37978974..37981398hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382425
hg192425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110628
Supporting Variants
Samplessample136
Known GenesMEAF6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096630
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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