A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613451



Internal ID20986522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99411958..99414850hg38UCSC Ensembl
chr7:99009581..99012473hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382893
hg192893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162417
Samples
Known GenesBUD31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613451
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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