A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371408



Internal ID22597077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63361017..63361017hg38UCSC Ensembl
chr18:61028250..61028250hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967570
Supporting Variants
Samples
Known GenesKDSR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371408
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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