A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035986



Internal ID19125205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81271207..81303967hg38UCSC Ensembl
Innerchr11:80982250..81015010hg19UCSC Ensembl
Innerchr11:80659898..80692658hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3832761
hg1932761
hg1832761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1241n100
Supporting Variantsnssv3503218
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)nsv1035986
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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