A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14340864



Internal ID22126562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35150828..35150893hg38UCSC Ensembl
chr10:35439756..35439821hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529300
Supporting Variants
SamplesHG00512
Known GenesCREM
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14340864
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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