A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3175599



Internal ID22333445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158146015..158150171hg38UCSC Ensembl
chr7:157938707..157942863hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg384157
hg194157
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14455710
SamplesHG00733
Known GenesPTPRN2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3175599
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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