A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17531701



Internal ID21856057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52688456..52688456hg38UCSC Ensembl
chr1:53154128..53154128hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg381335
hg191335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042349
Supporting Variants
Samples
Known GenesSELRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17531701
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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