A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044372



Internal ID20611412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9277706..9277818hg38UCSC Ensembl
chr18:9277704..9277816hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521230
Supporting Variants
Samples
Known GenesANKRD12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044372
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.05257


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