A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880597



Internal ID22655567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:232576916..232577013hg38UCSC Ensembl
chr1:232712662..232712759hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352265
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880597
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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