A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041811



Internal ID19131030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97103220..97176950hg38UCSC Ensembl
Innerchr11:96974220..97047950hg19UCSC Ensembl
Innerchr11:96479430..96553160hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3873731
hg1973731
hg1873731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1257n100
Supporting Variantsnssv3522478, nssv3516439, nssv3509398
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)nsv1041811
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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