A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045014



Internal ID19134233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46148750..46958662hg19UCSC Ensembl
Innerchr10:45468756..46378668hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg19809913
hg18909913
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv731n100
Supporting Variantsnssv3511527
Samples
Known GenesAGAP4, BMS1P1, BMS1P5, FAM21C, FAM35BP, FRMPD2P1, GLUD1P7, PTPN20A, PTPN20B, SYT15, ZFAND4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045014
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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