A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550404



Internal ID15991127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35600599..35673959hg38UCSC Ensembl
Innerchr10:35889527..35962887hg19UCSC Ensembl
Innerchr10:35929533..36002893hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3873361
hg1973361
hg1873361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1034n54
Supporting Variantsnssv1174984
Samples1780862415_A
Known GenesFZD8, GJD4, MIR4683
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550404
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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