A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14311904



Internal ID22122789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:192834829..192835456hg38UCSC Ensembl
chr3:192552618..192553245hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3207495
Supporting Variants
SamplesHG00512
Known GenesMB21D2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14311904
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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