A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425151



Internal ID21082704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157636687..158142155hg38UCSC Ensembl
chr7:157429379..157934847hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38505469
hg19505469
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217371
Samples
Known GenesLOC100506585, PTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425151
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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