A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378679



Internal ID21036232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39948986..39960215hg38UCSC Ensembl
chr5:39949088..39960317hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3811230
hg1911230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131458
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378679
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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