A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15185853



Internal ID21324665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3016165..3016165hg38UCSC Ensembl
chr18:3016163..3016163hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3937174
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15185853
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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