A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17632949



Internal ID21824996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45412465..45413030hg38UCSC Ensembl
chr19:45915723..45916288hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38566
hg19566
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054961
Supporting Variants
Samples
Known GenesERCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17632949
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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