A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054830



Internal ID18797361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46332711..46482057hg38UCSC Ensembl
Innerchr10:47067400..47249575hg19UCSC Ensembl
Innerchr10:46487406..46669581hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38149347
hg19182176
hg18182176
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv807n100
Supporting Variantsnssv3522662, nssv3522575
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)nsv1054830
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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