A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437329



Internal ID22103508
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 StatusM
Merged Variants
Supporting Variantsnssv15760226
Samples
Known GenesCDHR2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437329
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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