A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044361



Internal ID18786892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46526513..46631445hg38UCSC Ensembl
Innerchr10:46918172..47030888hg19UCSC Ensembl
Innerchr10:46338178..46450894hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38104933
hg19112717
hg18112717
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv748n100
Supporting Variantsnssv3514625, nssv3707862, nssv3707861, nssv3707860
Samples
Known GenesFAM35BP, 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)nsv1044361
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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