A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054931



Internal ID18797462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46395843..46489692hg38UCSC Ensembl
Innerchr10:47059745..47153919hg19UCSC Ensembl
Innerchr10:46479751..46573925hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3893850
hg1994175
hg1894175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv812n100
Supporting Variantsnssv3517950
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)nsv1054931
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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