A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611835



Internal ID20984906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102121465..102128225hg38UCSC Ensembl
chr7:101764745..101771505hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg386761
hg196761
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232610
Samples
Known GenesCUX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611835
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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