A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372168



Internal ID21029721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179094124..179099393hg38UCSC Ensembl
chr3:178811912..178817181hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg385270
hg195270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099748
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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