A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380751



Internal ID21038304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141435895..141436299hg38UCSC Ensembl
chr4:142357049..142357453hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108734
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380751
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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