A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027723



Internal ID21937066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30427367..30428061hg38UCSC Ensembl
chr16:30438688..30439382hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38695
hg19695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619668
Samples
Known GenesDCTPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027723
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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