A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14328778



Internal ID22196560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:82401525..82401682hg38UCSC Ensembl
chr6:83111242..83111399hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3200165
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14328778
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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