A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491765



Internal ID21149318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38835485..38852391hg38UCSC Ensembl
chr14:39304689..39321595hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3816907
hg1916907
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018185
Samples
Known GenesLINC00639
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491765
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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