A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616435



Internal ID20989506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123337150..123454647hg38UCSC Ensembl
chr6:123658295..123775792hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38117498
hg19117498
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214599
Samples
Known GenesTRDN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616435
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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