A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408565



Internal ID21066118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88128904..88157547hg38UCSC Ensembl
chr6:88838623..88867266hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3828644
hg1928644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229037
Samples
Known GenesCNR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408565
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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