A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14310752



Internal ID22259285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6725783..6725853hg38UCSC Ensembl
chr4:6727510..6727580hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3193457
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14310752
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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