A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15760226



Internal ID22094707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176591689..176591689hg38UCSC Ensembl
chr5:176018690..176018690hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4437329
Supporting Variants
Samples
Known GenesCDHR2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15760226
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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