A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14335645



Internal ID22210616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99385151..99390200hg38UCSC Ensembl
chr7:98982774..98987823hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg385050
hg195050
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3194387
Supporting Variants
SamplesHG00732
Known GenesARPC1B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14335645
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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