A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612953



Internal ID20986024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35253401..35254900hg38UCSC Ensembl
chr7:35293012..35294511hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219217
Samples
Known GenesTBX20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612953
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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