A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520090



Internal ID20893451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:7107797..7113948hg38UCSC Ensembl
chr18:7107796..7113947hg19UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg386152
hg196152
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197143
Samples
Known GenesLAMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520090
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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