A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14335751



Internal ID22182671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66392627..66395111hg38UCSC Ensembl
chr7:65857614..65860098hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg382485
hg192485
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3201438
Supporting Variants
SamplesHG00514
Known GenesLINC00174
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14335751
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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