A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613529



Internal ID20986600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73432358..73439868hg38UCSC Ensembl
chr7:72846688..72854198hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg387511
hg197511
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221967
Samples
Known GenesFZD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613529
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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