A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551044



Internal ID16338453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:55592021..55601042hg38UCSC Ensembl
Innerchr10:57351781..57360802hg19UCSC Ensembl
Innerchr10:57021787..57030808hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg389022
hg199022
hg189022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv748543
Samples
Known GenesMTRNR2L5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551044
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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