A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428754



Internal ID21086307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94874801..94877200hg38UCSC Ensembl
chr8:95887029..95889428hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171833
Samples
Known GenesINTS8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428754
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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