A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456132



Internal ID21113685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32240680..32255510hg38UCSC Ensembl
chr12:32393614..32408444hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3814831
hg1914831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000743
Samples
Known GenesBICD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456132
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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