A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849615



Internal ID22624550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:34203059..34208519hg38UCSC Ensembl
chr12:34355994..34361454hg19UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg385461
hg195461
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv364n209
Supporting Variantsnssv17451589, nssv17461635
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849615
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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