A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370971



Internal ID22596640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:82414980..82415095hg38UCSC Ensembl
chr1:82880663..82880778hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869690
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370971
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.015


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