A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552254



Internal ID15992977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122457306..122462027hg38UCSC Ensembl
Innerchr10:124216822..124221543hg19UCSC Ensembl
Innerchr10:124206812..124211533hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg384722
hg194722
hg184722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv760427, nssv760428
Samples
Known GenesARMS2, HTRA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552254
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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