A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881785



Internal ID22656761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:4136672..4140602hg38UCSC Ensembl
chr2:4184262..4188192hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg383931
hg193931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401312
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881785
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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