A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431471



Internal ID21089024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128241201..128278300hg38UCSC Ensembl
chr8:129253447..129290546hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3837100
hg1937100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7490n223
Supporting Variantsnssv18163837
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431471
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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