A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871654



Internal ID22646592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8187695..8190004hg38UCSC Ensembl
chr1:8247755..8250064hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg382310
hg192310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372248
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871654
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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