A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425934



Internal ID21083487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158332584..158341102hg38UCSC Ensembl
chr7:158125276..158133794hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg388519
hg198519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7204n223
Supporting Variantsnssv18152165
Samples
Known GenesPTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425934
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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