A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17530062



Internal ID21854418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19000002..19000002hg38UCSC Ensembl
chr1:19326496..19326496hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042370
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17530062
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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