A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485436



Internal ID21142989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:48438474..48501791hg38UCSC Ensembl
chr14:48907677..48970994hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3863318
hg1963318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019526
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485436
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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