A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382549



Internal ID21040102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:44102201..44103100hg38UCSC Ensembl
chr5:44102303..44103202hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132736
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382549
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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