A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13707497



Internal ID21229289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:65866004..65866347hg38UCSC Ensembl
chr18:63533240..63533583hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2798876
Supporting Variants
Samples
Known GenesCDH7
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13707497
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.890625


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