A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4021816



Internal ID22083447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:157545672..157558146hg38UCSC Ensembl
Outerchr7:157544783..157559061hg38UCSC Ensembl
Innerchr7:157338366..157350840hg19UCSC Ensembl
Outerchr7:157337477..157351755hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3814279
hg1914279
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156768
Supporting Variants
Samples
Known GenesPTPRN2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4021816
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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