A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489706



Internal ID21147259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:43384301..43764500hg38UCSC Ensembl
chr14:43853504..44233703hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38380200
hg19380200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2117n223
Supporting Variantsnssv18195190
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489706
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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