A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521422



Internal ID20894783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:7107790..7108431hg38UCSC Ensembl
chr18:7107789..7108430hg19UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197142
Samples
Known GenesLAMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521422
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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