A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932519



Internal ID22707819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:65543721..66206412hg38UCSC Ensembl
chr18:63210957..63873649hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38662692
hg19662693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381259
Samples
Known GenesCDH7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932519
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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