A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611192



Internal ID20984263
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 StatusM
Merged Variants
Supporting Variantsnssv18228612
Samples
Known GenesSH2B2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611192
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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