A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18158003



Internal ID20725043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66396260..66408653hg38UCSC Ensembl
chr7:65861247..65873640hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3812394
hg1912394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616309
Supporting Variants
Samples
Known GenesLINC00174
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18158003
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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