A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045680



Internal ID19134899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46395843..46472778hg38UCSC Ensembl
Innerchr10:47076675..47153919hg19UCSC Ensembl
Innerchr10:46496681..46573925hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3876936
hg1977245
hg1877245
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv819n100
Supporting Variantsnssv3508272, nssv3522251, nssv3705932, nssv3705933, nssv3517840
Samples
Known GenesHNRNPA1P33, 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)nsv1045680
Frequency
Sample Size11257
Observed Gain1
Observed Loss4
Observed Complex0
Frequencyn/a


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