A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732154



Internal ID20508077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2278343..2278399hg38UCSC Ensembl
chr19:2278342..2278398hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259852
Samples
Known GenesC19orf35
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732154
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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