A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18042763



Internal ID20609803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:7078408..7085605hg38UCSC Ensembl
chr18:7078407..7085604hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg387198
hg197198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525835
Supporting Variants
Samples
Known GenesLAMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18042763
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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