A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852909



Internal ID22627844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:117552281..117555196hg38UCSC Ensembl
chr7:117192335..117195250hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg382916
hg192916
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500730
Samples
Known GenesCFTR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852909
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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