A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225761



Internal ID22368794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8318115..8318727hg38UCSC Ensembl
chr19:8382999..8383611hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38613
hg19613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14285271
SamplesNA19240
Known GenesNDUFA7
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225761
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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