A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043498



Internal ID18786029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46407438..46481242hg38UCSC Ensembl
Innerchr10:47068215..47142310hg19UCSC Ensembl
Innerchr10:46488221..46562316hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3873805
hg1974096
hg1874096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv813n100
Supporting Variantsnssv3522454, nssv3705909
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)nsv1043498
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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