A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619247



Internal ID20992318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112017483..112054135hg38UCSC Ensembl
chr6:112338686..112375338hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3836653
hg1936653
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216823
Samples
Known GenesWISP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619247
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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