A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14334838



Internal ID22326554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95387997..95388084hg38UCSC Ensembl
chr7:95017309..95017396hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3193755
Supporting Variants
SamplesNA19240
Known GenesPON3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14334838
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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