A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205764



Internal ID22354408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:204184370..204184927hg38UCSC Ensembl
chr1:204153498..204154055hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14304387
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205764
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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