A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375671



Internal ID21033224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40252123..40256650hg38UCSC Ensembl
chr4:40253743..40258270hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg384528
hg194528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117097
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375671
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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