A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408895



Internal ID21066448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:118725528..118726050hg38UCSC Ensembl
chr5:118061223..118061745hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38523
hg19523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408895
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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