A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601228



Internal ID20974299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:69478668..69494628hg38UCSC Ensembl
chr7:68943654..68959614hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3815961
hg1915961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223666
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601228
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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