A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612598



Internal ID20985669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121789723..121798074hg38UCSC Ensembl
chr6:122110869..122119220hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg388352
hg198352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137579
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612598
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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