A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038522



Internal ID19127741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46332711..46489856hg38UCSC Ensembl
Innerchr10:47055642..47249575hg19UCSC Ensembl
Innerchr10:46475648..46669581hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38157146
hg19193934
hg18193934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv807n100
Supporting Variantsnssv3512517, nssv3503432
Samples
Known GenesAGAP9, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, HNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038522
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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