A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611847



Internal ID20984918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109381901..109382900hg38UCSC Ensembl
chr6:109703104..109704103hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216796
Samples
Known GenesCD164
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611847
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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