A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048865



Internal ID18791396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46529453..47024352hg38UCSC Ensembl
Innerchr10:46527665..47020164hg19UCSC Ensembl
Innerchr10:45947671..46440170hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38494900
hg19492500
hg18492500
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv734n100
Supporting Variantsnssv3519679
Samples
Known GenesBMS1P1, BMS1P5, FAM35BP, FRMPD2P1, GLUD1P7, GPRIN2, 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)nsv1048865
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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