A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18157113



Internal ID20724153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28984737..28994047hg38UCSC Ensembl
chr7:29024353..29033663hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg389311
hg199311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608663
Supporting Variants
Samples
Known GenesLOC100506497
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18157113
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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