A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616669



Internal ID20989740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101773536..102119723hg38UCSC Ensembl
chr7:101416816..101763003hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38346188
hg19346188
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220526
Samples
Known GenesCUX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616669
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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