A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264253



Internal ID20473471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:70302438..70302761hg38UCSC Ensembl
chr1:70768121..70768444hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741658
Supporting Variants
Samples
Known GenesANKRD13C
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264253
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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