A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14337749



Internal ID22186103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143359410..143360611hg38UCSC Ensembl
chr7:143056503..143057704hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV duplication
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3226238
Supporting Variants
SamplesHG00731
Known GenesFAM131B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14337749
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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