A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357767



Internal ID22583436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101855869..101861371hg38UCSC Ensembl
chr1:102321425..102326927hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg385503
hg195503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875815
Supporting Variants
Samples
Known GenesOLFM3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357767
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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