A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872099



Internal ID22647037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94713470..94713592hg38UCSC Ensembl
chr1:95179026..95179148hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409620
Samples
Known GenesLINC01057
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872099
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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