A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275160



Internal ID20842200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146170146..146170827hg38UCSC Ensembl
chr7:145867238..145867919hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38682
hg19682
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575558
Supporting Variants
Samples
Known GenesCNTNAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275160
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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