A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036156



Internal ID18778687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46395843..46489856hg38UCSC Ensembl
Innerchr10:47059174..47153919hg19UCSC Ensembl
Innerchr10:46479180..46573925hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3894014
hg1994746
hg1894746
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv803n100
Supporting Variantsnssv3503388
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)nsv1036156
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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