A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15764899



Internal ID22099380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46155803..46155803hg38UCSC Ensembl
chr12:46549586..46549586hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4437560
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15764899
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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