A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618073



Internal ID20991144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102694855..102763448hg38UCSC Ensembl
chr7:102335302..102403895hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3868594
hg1968594
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233620
Samples
Known GenesFAM185A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618073
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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