A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884118



Internal ID22659100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42834432..42835273hg38UCSC Ensembl
chr1:43300103..43300944hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38842
hg19842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385960
Samples
Known GenesERMAP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884118
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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