A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012067



Internal ID19101285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:114626816..114643410hg38UCSC Ensembl
Innerchr2:115384393..115400987hg19UCSC Ensembl
Innerchr2:115100863..115117457hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3816595
hg1916595
hg1816595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4054n100
Supporting Variantsnssv3580257, nssv3580245, nssv3580243, nssv3580254, nssv3580251, nssv3580249, nssv3580247, nssv3580256, nssv3580248, nssv3580250, nssv3580255, nssv3580252, nssv3580246, nssv3580258, nssv3580244, nssv3580253
Samples
Known GenesDPP10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012067
Frequency
Sample Size11257
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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