A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14310355



Internal ID22259234
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3199914
Supporting Variants
SamplesNA19238
Known GenesXXYLT1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14310355
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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