A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180879



Internal ID20747919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33536154..33540311hg38UCSC Ensembl
chr9:33536152..33540309hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg384158
hg194158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441479
Supporting Variants
Samples
Known GenesANKRD18B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180879
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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