A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199914



Internal ID22349436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195205821..195206097hg38UCSC Ensembl
chr3:194926550..194926826hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14310355, nssv14310353, nssv14310352, nssv14310354
SamplesHG00512, NA19238, HG00733, HG00513
Known GenesXXYLT1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199914
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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