A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412877



Internal ID21070430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:111540995..111569028hg38UCSC Ensembl
chr5:110876693..110904726hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3828034
hg1928034
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213349
Samples
Known GenesSTARD4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412877
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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