A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609566



Internal ID20982637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25958367..26200716hg38UCSC Ensembl
chr7:25997987..26240336hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38242350
hg19242350
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224124
Samples
Known GenesHNRNPA2B1, NFE2L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609566
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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