A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3706170



Internal ID19004451
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 StatusS
Merged Variantsnsv1053404
Supporting Variants
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)nssv3706170
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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