A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390684



Internal ID21048237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:176643701..176645400hg38UCSC Ensembl
chr4:177564852..177566551hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114234
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390684
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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