A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415953



Internal ID21073506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:152845501..153112300hg38UCSC Ensembl
chr7:152542586..152809385hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38266800
hg19266800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7188n223
Supporting Variantsnssv18220808
Samples
Known GenesACTR3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415953
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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