A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617800



Internal ID20990871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111724501..111732300hg38UCSC Ensembl
chr7:111364557..111372356hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg387800
hg197800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228079
Samples
Known GenesDOCK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617800
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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