A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554197



Internal ID15994920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45651464..45657662hg38UCSC Ensembl
Innerchr11:45673014..45679212hg19UCSC Ensembl
Innerchr11:45629590..45635788hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg386199
hg196199
hg186199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv772788
Samples
Known GenesCHST1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554197
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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