A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851236



Internal ID22626171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44279855..44284854hg38UCSC Ensembl
chr11:44301405..44306404hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453564
Samples
Known GenesALX4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851236
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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