A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634347



Internal ID21826394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39515154..39517367hg38UCSC Ensembl
chr19:40005794..40008007hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382214
hg192214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6057920
Supporting Variants
Samples
Known GenesSELV
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634347
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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