A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18159003



Internal ID20726043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79261842..79262341hg38UCSC Ensembl
chr7:78891158..78891657hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612566
Supporting Variants
Samples
Known GenesMAGI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18159003
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00042


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