A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492987



Internal ID21150540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65088947..65090909hg38UCSC Ensembl
chr14:65555665..65557627hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg381963
hg191963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2175n223
Supporting Variantsnssv18020717
Samples
Known GenesLOC100506321, MAX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492987
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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