A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038611



Internal ID18781142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46526513..46878295hg38UCSC Ensembl
Innerchr10:46674168..47058976hg19UCSC Ensembl
Innerchr10:46094174..46478982hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38351783
hg19384809
hg18384809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv742n100
Supporting Variantsnssv3510268
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)nsv1038611
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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