A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18157985



Internal ID20725025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66174464..66180027hg38UCSC Ensembl
chr7:65639451..65645014hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg385564
hg195564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608729
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18157985
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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