A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032642



Internal ID21941985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10448868..10451021hg38UCSC Ensembl
chr16:10542725..10544878hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg382154
hg192154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608716
Samples
Known GenesATF7IP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032642
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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