A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031325



Internal ID19120547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8702933..8747030hg38UCSC Ensembl
Innerchr5:8703045..8747142hg19UCSC Ensembl
Innerchr5:8756045..8800142hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3844098
hg1944098
hg1844098
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5564n100
Supporting Variantsnssv3746423, nssv3636761, nssv3746421, nssv3746426, nssv3636750, nssv3636752, nssv3636767, nssv3636755, nssv3636759, nssv3636760, nssv3636751, nssv3636766, nssv3636746, nssv3746420, nssv3636758, nssv3636748, nssv3636743, nssv3636742, nssv3636749, nssv3636763, nssv3636757, nssv3636764, nssv3636747, nssv3636741, nssv3638087, nssv3746424, nssv3636753, nssv3636765, nssv3746425, nssv3636756, nssv3636762, nssv3746427, nssv3638088, nssv3636745, nssv3636744, nssv3636754, nssv3746422
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031325
Frequency
Sample Size11257
Observed Gain0
Observed Loss37
Observed Complex0
Frequencyn/a


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