A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428602



Internal ID21086155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53346001..53347900hg38UCSC Ensembl
chr8:54258561..54260460hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168375
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428602
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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