A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603976



Internal ID20977047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106110901..106113400hg38UCSC Ensembl
chr7:105751347..105753846hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7045n223
Supporting Variantsnssv18229816
Samples
Known GenesSYPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603976
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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