A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562700



Internal ID16350109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:91347886..91348865hg38UCSC Ensembl
Innerchr13:92000140..92001119hg19UCSC Ensembl
Innerchr13:90798141..90799120hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38980
hg19980
hg18980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3316n54
Supporting Variantsnssv817426, nssv817427, nssv817424, nssv817425
Samples
Known GenesMIR17HG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562700
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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