A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417240



Internal ID21074793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38181340..38185595hg38UCSC Ensembl
chr8:38038858..38043113hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg384256
hg194256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168937
Samples
Known GenesBAG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417240
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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