A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879662



Internal ID22654633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64397748..64413261hg38UCSC Ensembl
chr1:64863431..64878944hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3815514
hg1915514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377641
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879662
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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