A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15767329



Internal ID22101800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13925069..13925069hg38UCSC Ensembl
chr6:13925300..13925300hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4439487
Supporting Variants
Samples
Known GenesRNF182
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15767329
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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