A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3934564



Internal ID21354633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56397743..56397963hg38UCSC Ensembl
chr16:56431655..56431875hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15175876
SamplesHG002
Known GenesAMFR
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3934564
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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