A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610593



Internal ID20983664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26212101..26213300hg38UCSC Ensembl
chr7:26251721..26252920hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222243
Samples
Known GenesCBX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610593
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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