A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884825



Internal ID22659809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14496576..14496673hg38UCSC Ensembl
chr1:14823072..14823169hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358170
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884825
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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