A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000266



Internal ID19089483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:56825698..56853807hg38UCSC Ensembl
Innerchr1:57291371..57319480hg19UCSC Ensembl
Innerchr1:57063959..57092068hg18UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3828110
hg1928110
hg1828110
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3464183
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)nsv1000266
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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