A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614621



Internal ID20987692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25069857..25070754hg38UCSC Ensembl
chr7:25109476..25110373hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38898
hg19898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155049
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614621
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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