A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15766683



Internal ID22101156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15742606..15742606hg38UCSC Ensembl
chr3:15784113..15784113hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38770
hg19770
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4438756
Supporting Variants
Samples
Known GenesANKRD28
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15766683
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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