A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421798



Internal ID21079351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56076201..56086500hg38UCSC Ensembl
chr8:56988760..56999059hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3810300
hg1910300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7354n223
Supporting Variantsnssv18169172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421798
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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