A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603731



Internal ID20976802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154178301..154181400hg38UCSC Ensembl
chr6:154499435..154502534hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139141
Samples
Known GenesIPCEF1, OPRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603731
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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