A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379618



Internal ID21037171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:36505098..36588646hg38UCSC Ensembl
chr5:36505200..36588748hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3883549
hg1983549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131956
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379618
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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