A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002686



Internal ID19091903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:29294244..29372604hg38UCSC Ensembl
Innerchr1:29620756..29699116hg19UCSC Ensembl
Innerchr1:29493343..29571703hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3878361
hg1978361
hg1878361
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3465095
Samples
Known GenesPTPRU
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002686
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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