A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614119



Internal ID20987190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1247223..1265299hg38UCSC Ensembl
chr7:1286859..1304935hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3818077
hg1918077
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221518
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614119
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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