A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013276



Internal ID19102494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:81538064..81604844hg38UCSC Ensembl
Innerchr1:82003749..82070529hg19UCSC Ensembl
Innerchr1:81776337..81843117hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3866781
hg1966781
hg1866781
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3474785
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)nsv1013276
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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