A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612789



Internal ID20985860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:147521101..147522700hg38UCSC Ensembl
chr6:147842237..147843836hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217069
Samples
Known GenesSAMD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612789
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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