A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036727



Internal ID18779258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67744858..67964843hg38UCSC Ensembl
Innerchr11:67512329..67732314hg19UCSC Ensembl
Innerchr11:67268905..67488890hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38219986
hg19219986
hg18219986
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1216n100
Supporting Variantsnssv3507607, nssv3512770
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)nsv1036727
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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