A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061538



Internal ID19150757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:7730118..7762151hg38UCSC Ensembl
Innerchr18:7730116..7762149hg19UCSC Ensembl
Innerchr18:7720116..7752149hg18UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg3832034
hg1932034
hg1832034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3319n100
Supporting Variantsnssv3564092
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)nsv1061538
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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