A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551459



Internal ID16338868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69523734..69537212hg38UCSC Ensembl
Innerchr10:71283490..71296968hg19UCSC Ensembl
Innerchr10:70953496..70966974hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3813479
hg1913479
hg1813479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1254n54
Supporting Variantsnssv750067, nssv750063, nssv750062, nssv1174243, nssv750069, nssv1174244, nssv750060, nssv750072, nssv750071, nssv750073, nssv750064, nssv1174238, nssv750068, nssv750065, nssv1174242, nssv1174239, nssv750061, nssv1174241, nssv1174240, nssv750070, nssv750066
SamplesHGDP00717, HGDP00750, HGDP01312, HGDP00956, HGDP01333, HGDP01331, HGDP01038
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551459
Frequency
Sample Size17421
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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