A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834144



Internal ID22609079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9671849..9677993hg38UCSC Ensembl
chr2:9811978..9818122hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg386145
hg196145
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482969
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834144
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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