A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14278708



Internal ID22262908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:158143103..158192003hg38UCSC Ensembl
Outerchr7:157935795..157984695hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3830946
hg1930946
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3226998
Supporting Variants
SamplesNA19238
Known GenesPTPRN2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14278708
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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