A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049343



Internal ID18791874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46412752..46459209hg38UCSC Ensembl
Innerchr10:47090539..47136996hg19UCSC Ensembl
Innerchr10:46510545..46557002hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3846458
hg1946458
hg1846458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv818n100
Supporting Variantsnssv3515878
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)nsv1049343
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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