A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609606



Internal ID20982677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109367301..109368300hg38UCSC Ensembl
chr6:109688504..109689503hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137047
Samples
Known GenesCD164
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609606
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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