A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379674



Internal ID21037227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:179056117..179733847hg38UCSC Ensembl
chr4:179977271..180655000hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38677731
hg19677730
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212819
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379674
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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