A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141670



Internal ID340867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158298804..158343000hg38UCSC Ensembl
chr7:158091496..158135692hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3844197
hg1944197
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17006053
Samples
Known GenesPTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141670
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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