A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146199



Internal ID345404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95245186..95245265hg38UCSC Ensembl
chr14:95711523..95711602hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698631
Samples
Known GenesCLMN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146199
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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