A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609264



Internal ID20982335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25114759..25121771hg38UCSC Ensembl
chr7:25154378..25161390hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg387013
hg197013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155520
Samples
Known GenesCYCS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609264
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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