A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012206



Internal ID19101424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75598736hg38UCSC Ensembl
Innerchr3:75427095..75647887hg19UCSC Ensembl
Innerchr3:75509785..75730577hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38220793
hg19220793
hg18220793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4777n100
Supporting Variantsnssv3602728, nssv3602726, nssv3733667, nssv3733665, nssv3602729, nssv3602730, nssv3733666, nssv3602727, nssv3733664, nssv3733662, nssv3733663
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012206
Frequency
Sample Size11257
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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