A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036397



Internal ID19125616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67757710..67942321hg38UCSC Ensembl
Innerchr11:67525181..67709792hg19UCSC Ensembl
Innerchr11:67281757..67466368hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38184612
hg19184612
hg18184612
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1218n100
Supporting Variantsnssv3516462, nssv3502956
Samples
Known GenesFAM86C2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036397
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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