A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409705



Internal ID21067258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95748454..95749114hg38UCSC Ensembl
chr6:96196330..96196990hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149827
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409705
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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