A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610838



Internal ID20983909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66918476..66922744hg38UCSC Ensembl
chr7:66383463..66387731hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg384269
hg194269
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222817
Samples
Known GenesTMEM248
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610838
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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