A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047139



Internal ID19136358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47003692..47704625hg19UCSC Ensembl
Innerchr10:46423698..47174631hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19700934
hg18750934
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv787n100
Supporting Variantsnssv3515799, nssv3705769, nssv3513075
Samples
Known GenesAGAP9, ANTXRL, ANTXRLP1, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, FAM35DP, 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)nsv1047139
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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