A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053404



Internal ID19142623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82650973..82671167hg38UCSC Ensembl
Innerchr10:84410729..84430923hg19UCSC Ensembl
Innerchr10:84400709..84420903hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3820195
hg1920195
hg1820195
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv945n100
Supporting Variantsnssv3706170
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)nsv1053404
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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