A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616341



Internal ID20989412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65063347..65753061hg38UCSC Ensembl
chr7:64523725..65218048hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38689715
hg19694324
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6861n223
Supporting Variantsnssv18235123
Samples
Known GenesCCT6P1, CCT6P3, INTS4L2, LOC441242, ZNF92
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616341
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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