A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380749



Internal ID21038302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36758144..36759168hg38UCSC Ensembl
chr4:36759766..36760790hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381025
hg191025
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117011
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380749
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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