A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041475



Internal ID18784006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46572046..46631445hg38UCSC Ensembl
Innerchr10:46918172..46977571hg19UCSC Ensembl
Innerchr10:46338178..46397577hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3859400
hg1959400
hg1859400
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv747n100
Supporting Variantsnssv3519340, nssv3520191, nssv3508776, nssv3515728, nssv3503541
Samples
Known GenesFAM35BP, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041475
Frequency
Sample Size29084
Observed Gain1
Observed Loss4
Observed Complex0
Frequencyn/a


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