A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601953



Internal ID20975024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:122008681..122017935hg38UCSC Ensembl
chr6:122329827..122339081hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg389255
hg199255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137326
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601953
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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