A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3518326



Internal ID18469921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46402445..46481242hg38UCSC Ensembl
Innerchr10:47068215..47147302hg19UCSC Ensembl
Innerchr10:46488221..46567308hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3878798
hg1979088
hg1879088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048658
Supporting Variants
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)nssv3518326
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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