A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873643



Internal ID22648591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10894205..10896070hg38UCSC Ensembl
chr1:10954262..10956127hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381866
hg191866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357758
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873643
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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