A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608140



Internal ID21800187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31404815..31404906hg38UCSC Ensembl
chr12:31557749..31557840hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029530
Supporting Variants
Samples
Known GenesDENND5B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608140
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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