A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180187



Internal ID20747227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102762744..102765081hg38UCSC Ensembl
chr14:103229081..103231418hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg382338
hg192338
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510127
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180187
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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