A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391678



Internal ID21049231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103960926..103961632hg38UCSC Ensembl
chr4:104882083..104882789hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106245
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391678
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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