A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841200



Internal ID22616135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154337777..154339006hg38UCSC Ensembl
chr5:153717337..153718566hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg381230
hg191230
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496339
Samples
Known GenesGALNT10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841200
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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