A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3518922



Internal ID18470517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46450514..46489816hg38UCSC Ensembl
Innerchr10:47059621..47099248hg19UCSC Ensembl
Innerchr10:46479627..46519254hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3839303
hg1939628
hg1839628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050998
Supporting Variants
Samples
Known GenesLINC00842, 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)nssv3518922
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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