A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192608



Internal ID22343163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41001..79829hg38UCSC Ensembl
chr1:41001..79829hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3838829
hg1938829
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14322122, nssv14322125, nssv14322121, nssv14322119, nssv14322124, nssv14322120, nssv14322117, nssv14322123, nssv14322118
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesOR4F5
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192608
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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