A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465351



Internal ID22523240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72235014..72240841hg38UCSC Ensembl
chr11:71946058..71951885hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg385828
hg195828
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866870
Supporting Variants
Samples
Known GenesINPPL1, PHOX2A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465351
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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