A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881896



Internal ID22656872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:54986637..54986871hg38UCSC Ensembl
chr1:55452310..55452544hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382678
Samples
Known GenesTMEM61
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881896
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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