A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14335554



Internal ID22308505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98140130..98140197hg38UCSC Ensembl
chr7:97769442..97769509hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527832
Supporting Variants
SamplesNA19240
Known GenesLMTK2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14335554
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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