A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482115



Internal ID21139668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88189599..88190396hg38UCSC Ensembl
chr14:88655943..88656740hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021593
Samples
Known GenesKCNK10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482115
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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