A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3464909



Internal ID18714271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:43559459..43620498hg38UCSC Ensembl
Innerchr1:44025130..44086169hg19UCSC Ensembl
Innerchr1:43797717..43858756hg18UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3861040
hg1961040
hg1861040
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000970
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)nssv3464909
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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