A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878896



Internal ID22653862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3973429..3973649hg38UCSC Ensembl
chr1:4033489..4033709hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373649
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878896
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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