A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404953



Internal ID21062506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8434501..8437700hg38UCSC Ensembl
chr6:8434734..8437933hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235633
Samples
Known GenesLOC100506207, SLC35B3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404953
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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