A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379918



Internal ID21037471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139307787..139315970hg38UCSC Ensembl
chr4:140228941..140237124hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg388184
hg198184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108040
Samples
Known GenesNAA15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379918
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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