A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17383441



Internal ID22441311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:23613448..23614353hg38UCSC Ensembl
chr18:21193412..21194317hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38906
hg19906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943150
Supporting Variants
Samples
Known GenesANKRD29
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17383441
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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