A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042036



Internal ID18784567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46428386..47024352hg38UCSC Ensembl
Innerchr10:46527665..47121369hg19UCSC Ensembl
Innerchr10:45947671..46541375hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38595967
hg19593705
hg18593705
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv734n100
Supporting Variantsnssv3508918
Samples
Known GenesBMS1P1, BMS1P5, FAM35BP, FRMPD2P1, GLUD1P7, GPRIN2, LINC00842, LOC100996758, NPY4R, 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)nsv1042036
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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