A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761630



Internal ID22096126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64594564..64594564hg38UCSC Ensembl
chr11:64362036..64362036hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4446228
Supporting Variants
Samples
Known GenesSLC22A12
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761630
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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