A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875187



Internal ID22650143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:105001673..105004794hg38UCSC Ensembl
chr1:105544295..105547416hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg383122
hg193122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366086
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875187
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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