A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14329691



Internal ID22277469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11763162..11764267hg38UCSC Ensembl
chr10:11805161..11806266hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381106
hg191106
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3217849
Supporting Variants
SamplesNA19239
Known GenesECHDC3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14329691
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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