A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3517878



Internal ID18469473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46440224..46878295hg38UCSC Ensembl
Innerchr10:46674168..47109535hg19UCSC Ensembl
Innerchr10:46094174..46529541hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38438072
hg19435368
hg18435368
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044415
Supporting Variants
Samples
Known GenesBMS1P1, BMS1P5, FAM35BP, FRMPD2P1, GLUD1P7, GPRIN2, LINC00842, LOC100996758, NPY4R, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3517878
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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