A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055960



Internal ID21965193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35095599..35095860hg38UCSC Ensembl
chr19:35586503..35586764hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633881
Samples
Known GenesHPN-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055960
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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