A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036977



Internal ID18779508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46332711..46595134hg38UCSC Ensembl
Innerchr10:46954483..47249575hg19UCSC Ensembl
Innerchr10:46374489..46669581hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38262424
hg19295093
hg18295093
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv767n100
Supporting Variantsnssv3505642
Samples
Known GenesAGAP9, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, 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)nsv1036977
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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