A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618170



Internal ID20991241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:122114528..122115891hg38UCSC Ensembl
chr6:122435674..122437037hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg381364
hg191364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137339
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618170
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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