A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981699



Internal ID21891042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173378675..173378891hg38UCSC Ensembl
chr1:173347814..173348030hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535601
Samples
Known GenesLOC100506023
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981699
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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