A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17482735



Internal ID22540641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:227375607..227386944hg38UCSC Ensembl
chr2:228240323..228251660hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3811338
hg1911338
Variant TypeOTHER copy number variation
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832226
Supporting Variants
Samples
Known GenesTM4SF20
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17482735
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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