A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14362626



Internal ID22190873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38841589..38841789hg38UCSC Ensembl
chr1:39307261..39307461hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527011
Supporting Variants
SamplesHG00731
Known GenesRRAGC
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14362626
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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