A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103968



Internal ID22013201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9370063..9370063hg38UCSC Ensembl
chr19:9480739..9480739hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631853
Samples
Known GenesZNF177, ZNF559-ZNF177
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103968
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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