A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215125



Internal ID22361560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35095671..35095850hg38UCSC Ensembl
chr19:35586575..35586754hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14286388, nssv14286385, nssv14286387, nssv14286386
SamplesNA19238, HG00731, HG00732, HG00733
Known GenesHPN-AS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215125
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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