A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042606



Internal ID19131825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82380564..82439303hg38UCSC Ensembl
Innerchr10:84140320..84199059hg19UCSC Ensembl
Innerchr10:84130300..84189039hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3858740
hg1958740
hg1858740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv943n100
Supporting Variantsnssv3512378
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)nsv1042606
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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