A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608634



Internal ID20981705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121278077..121326506hg38UCSC Ensembl
chr6:121599223..121647652hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3848430
hg1948430
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214582
Samples
Known GenesTBC1D32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608634
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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