A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142709



Internal ID341910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157553844..157554470hg38UCSC Ensembl
chr7:157346538..157347164hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17007837
Samples
Known GenesPTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142709
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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