A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032505



Internal ID21941848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23614779..23616901hg38UCSC Ensembl
chr16:23626100..23628222hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg382123
hg192123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598335
Samples
Known GenesPALB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032505
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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