A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601150



Internal ID20974221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102152016..102154111hg38UCSC Ensembl
chr7:101795296..101797391hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382096
hg192096
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236457
Samples
Known GenesCUX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601150
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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