A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618388



Internal ID20991459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:47515779..47520622hg38UCSC Ensembl
chr7:47555377..47560220hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg384844
hg194844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155433
Samples
Known GenesTNS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618388
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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