A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619654



Internal ID20992725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22092518..22098603hg38UCSC Ensembl
chr7:22132136..22138221hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg386086
hg196086
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236106
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619654
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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