A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877789



Internal ID22652754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:76005385..76009333hg38UCSC Ensembl
chr2:76232511..76236459hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg383949
hg193949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390327
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877789
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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