A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477932



Internal ID22535833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38588412..38591763hg38UCSC Ensembl
chr18:36168376..36171727hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg383352
hg193352
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881955
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477932
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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