A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384577



Internal ID21042130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:176618089..176669308hg38UCSC Ensembl
chr4:177539240..177590459hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3851220
hg1951220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384577
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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