A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426593



Internal ID21084146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158332334..158342566hg38UCSC Ensembl
chr7:158125026..158135258hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3810233
hg1910233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7204n223
Supporting Variantsnssv18152164
Samples
Known GenesPTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426593
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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