A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488912



Internal ID21146465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:41002828..41016477hg38UCSC Ensembl
chr14:41472033..41485682hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3813650
hg1913650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018592
Samples
Known GenesLOC644919
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488912
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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