A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844044



Internal ID22618979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138329542..138331121hg38UCSC Ensembl
chr6:138650679..138652258hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg381580
hg191580
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501766
Samples
Known GenesKIAA1244
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844044
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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