A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197142



Internal ID20764182
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 StatusS
Merged Variantsnsv6521422
Supporting Variants
Samples
Known GenesLAMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197142
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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