A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14333892



Internal ID22277845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29268490..29268542hg38UCSC Ensembl
chr7:29308106..29308158hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197906
Supporting Variants
SamplesNA19239
Known GenesCHN2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14333892
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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