A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874499



Internal ID22649451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:73275857..73276886hg38UCSC Ensembl
chr2:73502985..73504014hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg381030
hg191030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393700
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874499
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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