A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617627



Internal ID20990698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155925588..155926394hg38UCSC Ensembl
chr6:156246722..156247528hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38807
hg19807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139844
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617627
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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