A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010411



Internal ID18752942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:144950111..145023143hg38UCSC Ensembl
Innerchr1:143982530..144058996hg19UCSC Ensembl
Innerchr1:142693888..142770353hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg3873033
hg1976467
hg1876466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv312n100
Supporting Variantsnssv3482779, nssv3489567
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)nsv1010411
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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