A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613371



Internal ID16400780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10075721..10101169hg38UCSC Ensembl
Innerchr9:10075721..10101169hg19UCSC Ensembl
Innerchr9:10065721..10091169hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3825449
hg1925449
hg1825449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12516n54
Supporting Variantsnssv1126964
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613371
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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