A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603426



Internal ID20976497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107881201..107893700hg38UCSC Ensembl
chr7:107521646..107534145hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3812500
hg1912500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226470
Samples
Known GenesDLD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603426
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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