A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15767512



Internal ID22101989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184235668..184235668hg38UCSC Ensembl
chr3:183953456..183953456hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4440130
Supporting Variants
Samples
Known GenesVWA5B2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15767512
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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