A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14330495



Internal ID22254370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12401141..12401317hg38UCSC Ensembl
chr10:12443140..12443316hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213891
Supporting Variants
SamplesNA19238
Known GenesCAMK1D
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14330495
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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