A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399509



Internal ID21057062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14297160..14302583hg38UCSC Ensembl
chr6:14297391..14302814hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg385424
hg195424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140192
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399509
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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