A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417603



Internal ID21075156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73751965..73771214hg38UCSC Ensembl
chr8:74664200..74683449hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3819250
hg1919250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417603
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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