A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833994



Internal ID22608929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61054608..61058460hg38UCSC Ensembl
chr2:61281743..61285595hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg383853
hg193853
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487542
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833994
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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