A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876913



Internal ID22651875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15144923..15147922hg38UCSC Ensembl
chr2:15285047..15288046hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394913
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876913
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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