A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615059



Internal ID20988130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160022601..160144000hg38UCSC Ensembl
chr6:160443633..160565032hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38121400
hg19121400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6468n223
Supporting Variantsnssv18216724
Samples
Known GenesIGF2R, LOC729603, SLC22A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615059
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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