A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083002



Internal ID21282894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:3714670..3721829hg38UCSC Ensembl
Innerchr6:3714904..3722063hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg387160
hg197160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112479
Supporting Variants
Samplessample333
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083002
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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