A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616315



Internal ID20989386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109438735..109439502hg38UCSC Ensembl
chr6:109759938..109760705hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38768
hg19768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136624
Samples
Known GenesPPIL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616315
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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