A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041893



Internal ID18784424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46526513..46878295hg38UCSC Ensembl
Innerchr10:46674168..47055642hg19UCSC Ensembl
Innerchr10:46094174..46475648hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38351783
hg19381475
hg18381475
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv740n100
Supporting Variantsnssv3514699, nssv3518901, nssv3506345, nssv3519155, nssv3516413, nssv3507329, nssv3511649, nssv3519311, nssv3515656, nssv3511925, nssv3510495
Samples
Known GenesBMS1P1, BMS1P5, FAM35BP, FRMPD2P1, GLUD1P7, GPRIN2, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041893
Frequency
Sample Size29084
Observed Gain10
Observed Loss1
Observed Complex0
Frequencyn/a


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