A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012282



Internal ID19101500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72302803..72362283hg38UCSC Ensembl
Innerchr1:72768486..72827966hg19UCSC Ensembl
Innerchr1:72541074..72600554hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3859481
hg1959481
hg1859481
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3474331
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)nsv1012282
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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