A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605540



Internal ID20978611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66477161..66589405hg38UCSC Ensembl
chr7:65942148..66054392hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38112245
hg19112245
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233553
Samples
Known GenesLOC493754
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605540
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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