A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052088



Internal ID18794619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46332711..46481242hg38UCSC Ensembl
Innerchr10:47068215..47249575hg19UCSC Ensembl
Innerchr10:46488221..46669581hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38148532
hg19181361
hg18181361
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv807n100
Supporting Variantsnssv3705913, nssv3705912
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)nsv1052088
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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