A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406314



Internal ID21063867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71225122..71225799hg38UCSC Ensembl
chr6:71934825..71935502hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145099
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406314
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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