A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3507425



Internal ID18805706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46975048..47102936hg19UCSC Ensembl
Innerchr10:46395054..46522942hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19127889
hg18127889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043880
Supporting Variants
Samples
Known GenesGPRIN2, 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)nssv3507425
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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