A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872295



Internal ID22647234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158292139..158301453hg38UCSC Ensembl
chr1:158261929..158271243hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg389315
hg199315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364535
Samples
Known GenesCD1C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872295
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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