A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606688



Internal ID20979759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:114917962..115068039hg38UCSC Ensembl
chr6:115239126..115389203hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38150078
hg19150078
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214509
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606688
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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