A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618328



Internal ID20991399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87064025..87083840hg38UCSC Ensembl
chr7:86693341..86713156hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3819816
hg1919816
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618328
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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