A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376419



Internal ID21033972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70456666..70465506hg38UCSC Ensembl
chr4:71322383..71331223hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg388841
hg198841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119118
Samples
Known GenesMUC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376419
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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