A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608971



Internal ID20982042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113252696..113253047hg38UCSC Ensembl
chr6:113573898..113574249hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137051
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608971
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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