A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14363038



Internal ID22271412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41531634..41531842hg38UCSC Ensembl
chr1:41997305..41997513hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3199981
Supporting Variants
SamplesNA19239
Known GenesHIVEP3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14363038
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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