A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3709062



Internal ID18660657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46407438..46588039hg38UCSC Ensembl
Innerchr10:46961578..47142310hg19UCSC Ensembl
Innerchr10:46381584..46562316hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38180602
hg19180733
hg18180733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051992
Supporting Variants
Samples
Known GenesGPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3709062
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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