A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381937



Internal ID21039490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:144262227..144263112hg38UCSC Ensembl
chr4:145183380..145184265hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38886
hg19886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110847
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381937
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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