A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17384131



Internal ID22442001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46727855..46732566hg38UCSC Ensembl
chr1:47193527..47198238hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg384712
hg194712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878711
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17384131
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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