A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381913



Internal ID21039466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44948201..44950700hg38UCSC Ensembl
chr4:44950218..44952717hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117597
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381913
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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