A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616808



Internal ID20989879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:126060034..126060422hg38UCSC Ensembl
chr6:126381180..126381568hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138712
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616808
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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