A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380686



Internal ID21038239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:44872169..44872572hg38UCSC Ensembl
chr5:44872271..44872674hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131557
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380686
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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