A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619185



Internal ID20992256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1823990..1844357hg38UCSC Ensembl
chr7:1863626..1883993hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3820368
hg1920368
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234969
Samples
Known GenesMAD1L1, MIR4655
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619185
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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