A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067394



Internal ID19156613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:7730118..7768538hg38UCSC Ensembl
Innerchr18:7730116..7768536hg19UCSC Ensembl
Innerchr18:7720116..7758536hg18UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg3838421
hg1938421
hg1838421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3319n100
Supporting Variantsnssv3725287
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)nsv1067394
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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