A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561622



Internal ID16349031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:49939012..49940038hg38UCSC Ensembl
Innerchr13:50513148..50514174hg19UCSC Ensembl
Innerchr13:49411149..49412175hg18UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg381027
hg191027
hg181027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3141n54
Supporting Variantsnssv810375, nssv810387, nssv810382, nssv810384, nssv810391, nssv810385, nssv810392, nssv810378, nssv810379, nssv810383, nssv810380, nssv810389, nssv810381, nssv810393, nssv810376, nssv810386, nssv810388, nssv810377, nssv810390
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561622
Frequency
Sample Size17421
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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