A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050225



Internal ID18792756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46332711..46631445hg38UCSC Ensembl
Innerchr10:46918172..47249575hg19UCSC Ensembl
Innerchr10:46338178..46669581hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38298735
hg19331404
hg18331404
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707893, nssv3521493, nssv3516874, nssv3506177, nssv3522011, nssv3516348, nssv3510366, nssv3707892
Samples
Known GenesAGAP9, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, FAM35BP, GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050225
Frequency
Sample Size29084
Observed Gain6
Observed Loss2
Observed Complex0
Frequencyn/a


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