A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552177



Internal ID16339586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:112353831..112356529hg38UCSC Ensembl
Innerchr10:114113589..114116287hg19UCSC Ensembl
Innerchr10:114103579..114106277hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg382699
hg192699
hg182699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1395n54
Supporting Variantsnssv758427
Samples
Known GenesGUCY2GP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552177
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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