A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617248



Internal ID20990319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14972101..14996600hg38UCSC Ensembl
chr7:15011726..15036225hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3824500
hg1924500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6594n223
Supporting Variantsnssv18237021
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617248
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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