A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15192895



Internal ID21331777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2019220..2019220hg38UCSC Ensembl
chr1:1950659..1950659hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3945747
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15192895
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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