A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612778



Internal ID20985849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:11463401..11466000hg38UCSC Ensembl
chr7:11503028..11505627hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149886
Samples
Known GenesTHSD7A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612778
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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