A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832716



Internal ID22607651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:211177631..211217505hg38UCSC Ensembl
chr2:212042356..212082230hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3839875
hg1939875
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489306
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832716
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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