A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15186933



Internal ID21325762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151769286..151769286hg38UCSC Ensembl
chr1:151741762..151741762hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3941704
Supporting Variants
SamplesHG002
Known GenesOAZ3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15186933
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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