A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611299



Internal ID20984370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136810729..136884014hg38UCSC Ensembl
chr6:137131867..137205152hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3873286
hg1973286
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216838
Samples
Known GenesPEX7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611299
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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