A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832226



Internal ID22607161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:227375607..227386944hg38UCSC Ensembl
chr2:228240323..228251660hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3811338
hg1911338
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482734, nssv17482735
Samples
Known GenesTM4SF20
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832226
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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