A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608193



Internal ID20981264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95360972..95372970hg38UCSC Ensembl
chr7:94990284..95002282hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3811999
hg1911999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161625
Samples
Known GenesPON3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608193
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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