A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834064



Internal ID22608999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:83763733..83799912hg38UCSC Ensembl
chr2:83990857..84027036hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3836180
hg1936180
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488149
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834064
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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