A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14325585



Internal ID22261080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36363390..36363390hg38UCSC Ensembl
chr6:36331167..36331167hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3564364
Supporting Variants
SamplesNA19238
Known GenesETV7
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14325585
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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