A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18042179



Internal ID20609219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50231101..50236200hg38UCSC Ensembl
chr18:47757471..47762570hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521085
Supporting Variants
Samples
Known GenesCCDC11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18042179
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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