A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180788



Internal ID20747828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97668627..97779865hg38UCSC Ensembl
chr14:98134964..98246202hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38111239
hg19111239
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500703
Supporting Variants
Samples
Known GenesLOC100129345
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180788
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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