A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477878



Internal ID21135431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39236655..39238006hg38UCSC Ensembl
chr14:39705859..39707210hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg381352
hg191352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018211
Samples
Known GenesMIA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477878
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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