A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407790



Internal ID21065343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87443412..87700431hg38UCSC Ensembl
chr6:88153130..88410149hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38257020
hg19257020
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222339
Samples
Known GenesAKIRIN2, C6orf165, ORC3, RARS2, SLC35A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407790
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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