A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428077



Internal ID21085630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97363162..97633802hg38UCSC Ensembl
chr8:98375390..98646030hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38270641
hg19270641
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231495
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428077
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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