A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418957



Internal ID21076510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64349538..64350101hg38UCSC Ensembl
chr8:65262095..65262658hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168821
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418957
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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