A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606624



Internal ID20979695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155864601..155869100hg38UCSC Ensembl
chr6:156185735..156190234hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216685
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606624
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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