A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064869



Internal ID19154088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:7730118..7760971hg38UCSC Ensembl
Innerchr18:7730116..7760969hg19UCSC Ensembl
Innerchr18:7720116..7750969hg18UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg3830854
hg1930854
hg1830854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3319n100
Supporting Variantsnssv3725285, nssv3564091, nssv3725284, nssv3725286, nssv3725283, nssv3725282
Samples
Known GenesPTPRM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064869
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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