A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778992



Internal ID15726262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:72694178..72730386hg38UCSC Ensembl
Innerchr11:72405223..72441431hg19UCSC Ensembl
Innerchr11:72082871..72119079hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3836209
hg1936209
hg1836209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555408
Supporting Variants
Samples
Known GenesARAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778992
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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