A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14324832



Internal ID22209060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2893191..2893191hg38UCSC Ensembl
chr6:2893425..2893425hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3564642
Supporting Variants
SamplesHG00732
Known GenesSERPINB9
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14324832
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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