A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382371



Internal ID21039924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174584101..174588300hg38UCSC Ensembl
chr4:175505252..175509451hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212767
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382371
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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