A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607012



Internal ID20980083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:11470301..11471800hg38UCSC Ensembl
chr7:11509928..11511427hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149903
Samples
Known GenesTHSD7A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607012
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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