A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14322121



Internal ID22208954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41001..79829hg38UCSC Ensembl
chr1:41001..79829hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3838829
hg1938829
Variant TypeOTHER copy number variation
Copy Number8
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3192608
Supporting Variants
SamplesHG00732
Known GenesOR4F5
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14322121
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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