A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610862



Internal ID21802909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32133456..32142166hg38UCSC Ensembl
chr12:32286390..32295100hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg388711
hg198711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028707
Supporting Variants
Samples
Known GenesBICD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610862
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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