A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043778



Internal ID18786309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46568009..46861290hg38UCSC Ensembl
Innerchr10:46691159..46981608hg19UCSC Ensembl
Innerchr10:46111165..46401614hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38293282
hg19290450
hg18290450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv742n100
Supporting Variantsnssv3507331
Samples
Known GenesBMS1P1, BMS1P5, FAM35BP, GLUD1P7, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043778
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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