A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047088



Internal ID18789619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46411170..46453530hg38UCSC Ensembl
Innerchr10:47096230..47138582hg19UCSC Ensembl
Innerchr10:46516236..46558588hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3842361
hg1942353
hg1842353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516859
Samples
Known GenesHNRNPA1P33, LINC00842
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047088
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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