A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3477439



Internal ID18720870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:43560418..43620498hg38UCSC Ensembl
Innerchr1:44026089..44086169hg19UCSC Ensembl
Innerchr1:43798676..43858756hg18UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3860081
hg1960081
hg1860081
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008451
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)nssv3477439
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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