A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423444



Internal ID21080997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:52793405..53115793hg38UCSC Ensembl
chr8:53705965..54028353hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38322389
hg19322389
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234537
Samples
Known GenesNPBWR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423444
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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