A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259852



Internal ID20469070
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 StatusS
Merged Variantsnsv4732154
Supporting Variants
Samples
Known GenesC19orf35
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259852
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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