A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14355909



Internal ID22283653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124945923..124946309hg38UCSC Ensembl
chr10:126634492..126634878hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3230222
Supporting Variants
SamplesNA19239
Known GenesZRANB1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14355909
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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