A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054174



Internal ID18796705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46402445..46560537hg38UCSC Ensembl
Innerchr10:46989080..47147302hg19UCSC Ensembl
Innerchr10:46409086..46567308hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38158093
hg19158223
hg18158223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv781n100
Supporting Variantsnssv3705746
Samples
Known GenesGPRIN2, HNRNPA1P33, 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)nsv1054174
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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