A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377753



Internal ID21035306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5803747..5810545hg38UCSC Ensembl
chr5:5803860..5810658hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg386799
hg196799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133632
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377753
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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