A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17384715



Internal ID22442585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4850508..4850508hg38UCSC Ensembl
chr18:4850507..4850507hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5969255
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17384715
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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