A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408363



Internal ID21065916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:98201765..98216851hg38UCSC Ensembl
chr5:97537469..97552555hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3815087
hg1915087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136560
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408363
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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