A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045120



Internal ID19134339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46215431..46977571hg19UCSC Ensembl
Innerchr10:45535437..46397577hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg19762141
hg18862141
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv731n100
Supporting Variantsnssv3507941
Samples
Known GenesAGAP4, BMS1P1, BMS1P5, FAM21C, FAM35BP, FRMPD2P1, GLUD1P7, PTPN20A, PTPN20B, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045120
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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