A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040321



Internal ID21949664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51319097..51322000hg38UCSC Ensembl
chr12:51712881..51715784hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg382904
hg192904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609733
Samples
Known GenesBIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040321
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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