A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038276



Internal ID18780807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46554143..46631445hg38UCSC Ensembl
Innerchr10:46918172..46995474hg19UCSC Ensembl
Innerchr10:46338178..46415480hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3877303
hg1977303
hg1877303
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv747n100
Supporting Variantsnssv3513118, nssv3519769, nssv3517048
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)nsv1038276
Frequency
Sample Size29084
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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