A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3195844



Internal ID22345958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181897360..181897998hg38UCSC Ensembl
chr3:181615148..181615786hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14310141, nssv14310142
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3195844
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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