A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396900



Internal ID21054453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87581244..87584816hg38UCSC Ensembl
chr5:86877061..86880633hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg383573
hg193573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134730
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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