A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151862



Internal ID15879742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8784337..8821239hg38UCSC Ensembl
Innerchr3:8826023..8862925hg19UCSC Ensembl
Innerchr3:8801023..8837925hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3836903
hg1936903
hg1836903
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589632
Supporting Variants
SamplesNINDS_102
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151862
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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