A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14325005



Internal ID22267297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10274673..10274759hg38UCSC Ensembl
chr1:10334731..10334817hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525909
Supporting Variants
SamplesNA19238
Known GenesKIF1B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14325005
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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