A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616053



Internal ID20989124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40099808..40238833hg38UCSC Ensembl
chr7:40139407..40278432hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38139026
hg19139026
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235760
Samples
Known GenesC7orf10, MPLKIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616053
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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