A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872904



Internal ID22647846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:112179208..112179427hg38UCSC Ensembl
chr1:112721830..112722049hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364719
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872904
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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