A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372111



Internal ID22597780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32821353..32821665hg38UCSC Ensembl
chr1:33286954..33287266hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869466
Supporting Variants
Samples
Known GenesS100PBP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372111
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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