A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035306



Internal ID18777837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71615895..71812505hg38UCSC Ensembl
Innerchr11:71326941..71523551hg19UCSC Ensembl
Innerchr11:71004589..71201199hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38196611
hg19196611
hg18196611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1222n100
Supporting Variantsnssv3710649
Samples
Known GenesALG1L9P, FAM86C1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035306
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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