A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560013



Internal ID16347422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:101711211..101713222hg38UCSC Ensembl
Innerchr12:102104989..102107000hg19UCSC Ensembl
Innerchr12:100629120..100631131hg18UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg382012
hg192012
hg182012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2835n54
Supporting Variantsnssv801719, nssv801718, nssv801714, nssv801709, nssv801687, nssv801691, nssv801690, nssv801685, nssv801705, nssv801698, nssv801694, nssv801696, nssv801695, nssv801712, nssv801708, nssv801706, nssv801710, nssv801713, nssv801711, nssv801693, nssv801697, nssv801720, nssv801686, nssv801704, nssv801703, nssv801688, nssv801702, nssv801689, nssv801716, nssv801715, nssv801701, nssv801700, nssv801692, nssv801707, nssv801717, nssv801699, nssv801684
Samples
Known GenesCHPT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560013
Frequency
Sample Size17421
Observed Gain0
Observed Loss37
Observed Complex0
Frequencyn/a


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