A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14335624



Internal ID22241099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99190284..99190717hg38UCSC Ensembl
chr7:98787907..98788340hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206830
Supporting Variants
SamplesHG00733
Known GenesKPNA7
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14335624
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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