A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3471484



Internal ID19064482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38n/a
hg19n/a
hg18n/a
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004888
Supporting Variants
Samples
Known GenesPTPRF
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3471484
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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