A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429082



Internal ID21086635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158146094..158283815hg38UCSC Ensembl
chr7:157938786..158076507hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38137722
hg19137722
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220577
Samples
Known GenesPTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429082
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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