A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15766221



Internal ID22100692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185453787..185453843hg38UCSC Ensembl
chr3:185171575..185171631hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4445655
Supporting Variants
Samples
Known GenesMAP3K13
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15766221
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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