A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14331622



Internal ID22195498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113621725..113621819hg38UCSC Ensembl
chr6:113942927..113943021hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3193220
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14331622
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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