A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842877



Internal ID22617812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79079292..79093835hg38UCSC Ensembl
chr5:78375115..78389658hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3814544
hg1914544
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498735
Samples
Known GenesBHMT2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842877
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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