A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277323



Internal ID20486541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56149068..56149178hg38UCSC Ensembl
chr19:56660437..56660547hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738433
Supporting Variants
Samples
Known GenesZNF444
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277323
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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