A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047857



Internal ID18790388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46428386..46602921hg38UCSC Ensembl
Innerchr10:46946696..47121369hg19UCSC Ensembl
Innerchr10:46366702..46541375hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38174536
hg19174674
hg18174674
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv753n100
Supporting Variantsnssv3514376
Samples
Known GenesGPRIN2, 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)nsv1047857
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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