A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893936



Internal ID22669004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142000811..142098591hg38UCSC Ensembl
chr6:142321948..142419728hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3897781
hg1997781
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414578
Samples
Known GenesNMBR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893936
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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