A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036520



Internal ID18779051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46407438..46878295hg38UCSC Ensembl
Innerchr10:46674168..47142310hg19UCSC Ensembl
Innerchr10:46094174..46562316hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38470858
hg19468143
hg18468143
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv740n100
Supporting Variantsnssv3509799, nssv3519134, nssv3504995
Samples
Known GenesBMS1P1, BMS1P5, FAM35BP, FRMPD2P1, GLUD1P7, GPRIN2, HNRNPA1P33, 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)nsv1036520
Frequency
Sample Size29084
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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