A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552176



Internal ID16339585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:112353831..112356418hg38UCSC Ensembl
Innerchr10:114113589..114116176hg19UCSC Ensembl
Innerchr10:114103579..114106166hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg382588
hg192588
hg182588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1395n54
Supporting Variantsnssv758426
Samples
Known GenesGUCY2GP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552176
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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