A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391582



Internal ID21049135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70109399..70169820hg38UCSC Ensembl
chr4:70975116..71035537hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3860422
hg1960422
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5325n223
Supporting Variantsnssv18211710
Samples
Known GenesC4orf40, CSN1S2BP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391582
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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