A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044358



Internal ID20611398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9168055..9172742hg38UCSC Ensembl
chr18:9168053..9172740hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg384688
hg194688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519323
Supporting Variants
Samples
Known GenesANKRD12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044358
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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