A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372020



Internal ID22597689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86348641..86353154hg38UCSC Ensembl
chr1:86814324..86818837hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg384514
hg194514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877988
Supporting Variants
Samples
Known GenesODF2L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372020
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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