A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041060



Internal ID18783591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46332711..46487142hg38UCSC Ensembl
Innerchr10:47062299..47249575hg19UCSC Ensembl
Innerchr10:46482305..46669581hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38154432
hg19187277
hg18187277
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518449, nssv3705861, nssv3513308, nssv3515737, nssv3521105
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)nsv1041060
Frequency
Sample Size29084
Observed Gain3
Observed Loss2
Observed Complex0
Frequencyn/a


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