A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844013



Internal ID22618948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125702180..125707345hg38UCSC Ensembl
chr6:126023326..126028491hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg385166
hg195166
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501555
Samples
Known GenesLOC643623
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844013
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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