A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17400907



Internal ID22458777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9284981..9286147hg38UCSC Ensembl
chr18:9284979..9286145hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381167
hg191167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937029
Supporting Variants
Samples
Known GenesANKRD12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17400907
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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