A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869690



Internal ID22644625
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 StatusM
Merged Variants
Supporting Variantsnssv17370971
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869690
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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