A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522510



Internal ID15103117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132011133..132012913hg38UCSC Ensembl
Innerchr11:131881027..131882807hg19UCSC Ensembl
Innerchr11:131386237..131388017hg18UCSC Ensembl
Innerchr11:131386237..131388017hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381781
hg191781
hg181781
hg171781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705878
Samples
Known GenesNTM
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522510
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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