A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602286



Internal ID20975357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:114472499..114708262hg38UCSC Ensembl
chr6:114793663..115029426hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38235764
hg19235764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138066
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602286
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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