A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14330757



Internal ID22146754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107100301..107101140hg38UCSC Ensembl
chr6:107421505..107422344hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38840
hg19840
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206541
Supporting Variants
SamplesHG00514
Known GenesBEND3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14330757
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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