A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614946



Internal ID20988017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87184732..87185280hg38UCSC Ensembl
chr7:86814048..86814596hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38549
hg19549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161745
Samples
Known GenesDMTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614946
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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