A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610669



Internal ID20983740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137288000..137444045hg38UCSC Ensembl
chr6:137609137..137765182hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38156046
hg19156046
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216847
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610669
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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