A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617428



Internal ID20990499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:94700401..94707900hg38UCSC Ensembl
chr7:94329713..94337212hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7012n223
Supporting Variantsnssv18219750
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617428
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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