A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049033



Internal ID19138252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82417429..82500287hg38UCSC Ensembl
Innerchr10:84177185..84260043hg19UCSC Ensembl
Innerchr10:84167165..84250023hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3882859
hg1982859
hg1882859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3519827
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)nsv1049033
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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