A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842486



Internal ID22617421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177599102..177609949hg38UCSC Ensembl
chr5:177026103..177036950hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3810848
hg1910848
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494974
Samples
Known GenesB4GALT7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842486
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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