A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409265



Internal ID21066818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84012801..84044400hg38UCSC Ensembl
chr6:84722520..84754119hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg3831600
hg1931600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227062
Samples
Known GenesMRAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409265
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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