A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381591



Internal ID21039144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:178005724..178006241hg38UCSC Ensembl
chr4:178926878..178927395hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38518
hg19518
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212800
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381591
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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