A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396315



Internal ID21053868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:121853455..121883507hg38UCSC Ensembl
chr5:121189150..121219202hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3830053
hg1930053
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213127
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396315
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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