A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18157716



Internal ID20724756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:52770841..52771460hg38UCSC Ensembl
chr7:52838535..52839154hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614004
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18157716
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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