A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14378966



Internal ID22126618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25999825..25999895hg38UCSC Ensembl
chr15:26244972..26245042hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3214886
Supporting Variants
SamplesHG00512
Known GenesLOC100128714
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14378966
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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