A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042769



Internal ID19131988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97107874..97229891hg38UCSC Ensembl
Innerchr11:96978874..97100891hg19UCSC Ensembl
Innerchr11:96484084..96606101hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38122018
hg19122018
hg18122018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1258n100
Supporting Variantsnssv3507866, nssv3510014
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)nsv1042769
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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