A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619355



Internal ID20992426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65035202..65870265hg38UCSC Ensembl
chr7:64495580..65335252hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38835064
hg19839673
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6861n223
Supporting Variantsnssv18221554
Samples
Known GenesCCT6P1, CCT6P3, INTS4L2, LOC441242, SNORA22, ZNF92
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619355
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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