A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14296909



Internal ID22126851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178526150..178526503hg38UCSC Ensembl
chr1:178495285..178495638hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525428
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14296909
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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