A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406604



Internal ID21064157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:84852633..84907913hg38UCSC Ensembl
chr5:84148451..84203731hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3855281
hg1955281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133991
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406604
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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