A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228612



Internal ID20795652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102319287..102334951hg38UCSC Ensembl
chr7:101959754..101975364hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3815665
hg1915611
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611192
Supporting Variants
Samples
Known GenesSH2B2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228612
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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