A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057760



Internal ID19146979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:7732190..7760971hg38UCSC Ensembl
Innerchr18:7732188..7760969hg19UCSC Ensembl
Innerchr18:7722188..7750969hg18UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg3828782
hg1928782
hg1828782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3319n100
Supporting Variantsnssv3564094, nssv3564093
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)nsv1057760
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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