A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385335



Internal ID22443205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4668078..4687110hg38UCSC Ensembl
chr18:4668078..4687110hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3819033
hg1919033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934318
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385335
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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