A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561176



Internal ID21885531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3978410..3978476hg38UCSC Ensembl
chr6:3978644..3978710hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014087
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561176
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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