A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15192254



Internal ID21331064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60982123..60982123hg38UCSC Ensembl
chr11:60749595..60749595hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3934979
Supporting Variants
SamplesHG002
Known GenesCD6
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15192254
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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