A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866870



Internal ID22641805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72235014..72240841hg38UCSC Ensembl
chr11:71946058..71951885hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg385828
hg195828
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465351
Samples
Known GenesINPPL1, PHOX2A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866870
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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