A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419900



Internal ID21077453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73175176..73175653hg38UCSC Ensembl
chr8:74087411..74087888hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170358
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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