A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17482624



Internal ID22540530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:213605586..213617447hg38UCSC Ensembl
chr2:214470310..214482171hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3811862
hg1911862
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832726
Supporting Variants
Samples
Known GenesSPAG16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17482624
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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