A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15201655



Internal ID21340455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3356090..3356090hg38UCSC Ensembl
chr6:3356324..3356324hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3939113
Supporting Variants
SamplesHG002
Known GenesSLC22A23
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15201655
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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