A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051317



Internal ID19140536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82503688..82574754hg38UCSC Ensembl
Innerchr10:84263444..84334510hg19UCSC Ensembl
Innerchr10:84253424..84324490hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3871067
hg1971067
hg1871067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520384, nssv3522528
Samples
Known GenesNRG3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051317
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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