A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15766794



Internal ID22101267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34157878..34157959hg38UCSC Ensembl
chr17:32484897..32484978hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4437404
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15766794
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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