A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406295



Internal ID21063848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:77831637..78599649hg38UCSC Ensembl
chr6:78541354..79309366hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38768013
hg19768013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148938
Samples
Known GenesMEI4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406295
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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