A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14359929



Internal ID22303158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33474705..33483677hg38UCSC Ensembl
chr1:33940306..33949277hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg388973
hg198972
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3245115
Supporting Variants
SamplesNA19240
Known GenesZSCAN20
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14359929
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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