A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875354



Internal ID22650311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8876621..8877578hg38UCSC Ensembl
chr1:8936680..8937637hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38958
hg19958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393749
Samples
Known GenesENO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875354
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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