A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385609



Internal ID22443479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61262565..61267015hg38UCSC Ensembl
chr18:58929798..58934248hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg384451
hg194451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940156
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385609
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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