A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615701



Internal ID20988772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107112712..107160127hg38UCSC Ensembl
chr6:107433916..107481331hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3847416
hg1947416
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216573
Samples
Known GenesBEND3, PDSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615701
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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