A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004186



Internal ID19093403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:90669710..90704630hg38UCSC Ensembl
Innerchr1:91135267..91170187hg19UCSC Ensembl
Innerchr1:90907855..90942775hg18UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3834921
hg1934921
hg1834921
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3468139
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004186
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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