A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605727



Internal ID20978798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:11472455..11558492hg38UCSC Ensembl
chr7:11512082..11598119hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3886038
hg1986038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149905
Samples
Known GenesTHSD7A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605727
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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