A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047575



Internal ID19136794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:42265498..42305603hg38UCSC Ensembl
Innerchr11:42287048..42327153hg19UCSC Ensembl
Innerchr11:42243624..42283729hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3840106
hg1940106
hg1840106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1107n100
Supporting Variantsnssv3510634, nssv3505812, nssv3507294, nssv3521072
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)nsv1047575
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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