A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15764446



Internal ID22098919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71999674..71999674hg38UCSC Ensembl
chr14:72466391..72466391hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4445405
Supporting Variants
Samples
Known GenesRGS6
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15764446
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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