A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14331235



Internal ID22207802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151498890..151499363hg38UCSC Ensembl
chr6:151820025..151820498hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197952
Supporting Variants
SamplesHG00732
Known GenesCCDC170
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14331235
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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