A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037631



Internal ID19126850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134992302..135074876hg38UCSC Ensembl
Innerchr11:134862196..134944770hg19UCSC Ensembl
Innerchr11:134367406..134449982hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3882575
hg1982575
hg1882577
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1320n100
Supporting Variantsnssv3505248, nssv3521254
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)nsv1037631
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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