A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18158002



Internal ID20725042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66392587..66395177hg38UCSC Ensembl
chr7:65857574..65860164hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg382591
hg192591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609497
Supporting Variants
Samples
Known GenesLINC00174
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18158002
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.46986


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