A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551544



Internal ID15992267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:76496115..76500936hg38UCSC Ensembl
Innerchr10:78255873..78260694hg19UCSC Ensembl
Innerchr10:77925879..77930700hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg384822
hg194822
hg184822
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1269n54
Supporting Variantsnssv751720, nssv751717, nssv751716, nssv751722, nssv751713, nssv751705, nssv751724, nssv751707, nssv751711, nssv751719, nssv751723, nssv751718, nssv751712, nssv751706, nssv751715, nssv751709, nssv751708, nssv751714, nssv751721, nssv751710
Samples
Known GenesC10orf11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551544
Frequency
Sample Size17421
Observed Gain19
Observed Loss1
Observed Complex0
Frequencyn/a


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