A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832974



Internal ID22607909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36883447..36914888hg38UCSC Ensembl
chr2:37110590..37142031hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3831442
hg1931442
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484783
Samples
Known GenesSTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832974
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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