A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550405



Internal ID15991128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35612787..35673959hg38UCSC Ensembl
Innerchr10:35901715..35962887hg19UCSC Ensembl
Innerchr10:35941721..36002893hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3861173
hg1961173
hg1861173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1034n54
Supporting Variantsnssv1174985
Samples1780862275_A
Known GenesFZD8, MIR4683
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550405
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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