A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432946



Internal ID21090499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100938801..100960700hg38UCSC Ensembl
chr8:101951029..101972928hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3821900
hg1921900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218611
Samples
Known GenesYWHAZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432946
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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