A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016761



Internal ID19105978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:87129228..87284836hg38UCSC Ensembl
Innerchr7:86758544..86914152hg19UCSC Ensembl
Innerchr7:86596480..86752088hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38155609
hg19155609
hg18155609
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655187
Samples
Known GenesDMTF1, TMEM243
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016761
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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