A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14336921



Internal ID22198860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137946924..137946976hg38UCSC Ensembl
chr7:137631670..137631722hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3212017
Supporting Variants
SamplesHG00732
Known GenesCREB3L2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14336921
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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