A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854889



Internal ID22629824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148164731..148165830hg38UCSC Ensembl
chr7:147861823..147862922hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504569
Samples
Known GenesCNTNAP2, MIR548T
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854889
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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