A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15204314



Internal ID21343117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:159018226..159018226hg38UCSC Ensembl
chr7:158810917..158810917hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38656
hg19656
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3943613
Supporting Variants
SamplesHG002
Known GenesLINC00689
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15204314
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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