A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390406



Internal ID21047959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70336687..70336913hg38UCSC Ensembl
chr4:71202404..71202630hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211717
Samples
Known GenesCABS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390406
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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