A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17535757



Internal ID21860112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:219546012..219546012hg38UCSC Ensembl
chr1:219719354..219719354hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056380
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17535757
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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