A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423351



Internal ID21080904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9800030..9812013hg38UCSC Ensembl
chr8:9657540..9669523hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3811984
hg1911984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173578
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423351
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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