A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3516297



Internal ID18467892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46446826..46878295hg38UCSC Ensembl
Innerchr10:46674168..47102936hg19UCSC Ensembl
Innerchr10:46094174..46522942hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38431470
hg19428769
hg18428769
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044607
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)nssv3516297
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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