A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14355805



Internal ID22142028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23734039..23734788hg38UCSC Ensembl
chr1:24060529..24061278hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38750
hg19750
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3208642
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14355805
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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