A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385122



Internal ID22442992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60121856..60121856hg38UCSC Ensembl
chr1:60587528..60587528hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5959063
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385122
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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