A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144164



Internal ID343368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:48187537..48192837hg38UCSC Ensembl
chr14:48656740..48662040hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg385301
hg195301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17694806
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144164
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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