A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18161277



Internal ID20728317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98485120..98516365hg38UCSC Ensembl
chr7:98114432..98145677hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3831246
hg1931246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617635
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18161277
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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