A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3505690



Internal ID18457285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46432210..46588384hg38UCSC Ensembl
Innerchr10:46961233..47117543hg19UCSC Ensembl
Innerchr10:46381239..46537549hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38156175
hg19156311
hg18156311
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038133
Supporting Variants
Samples
Known GenesGPRIN2, 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)nssv3505690
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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