A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606893



Internal ID20979964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77520975..77581052hg38UCSC Ensembl
chr7:77150292..77210369hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3860078
hg1960078
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221819
Samples
Known GenesPTPN12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606893
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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