A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042924



Internal ID19132143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76948433..77017224hg38UCSC Ensembl
Innerchr11:76659477..76728268hg19UCSC Ensembl
Innerchr11:76337125..76405916hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3868792
hg1968792
hg1868792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1229n100
Supporting Variantsnssv3514568
Samples
Known GenesACER3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042924
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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