A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613374



Internal ID20986445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32169694..32385530hg38UCSC Ensembl
chr7:32209306..32425142hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38215837
hg19215837
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226867
Samples
Known GenesPDE1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613374
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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