A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048978



Internal ID19138197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82650973..82673635hg38UCSC Ensembl
Innerchr10:84410729..84433391hg19UCSC Ensembl
Innerchr10:84400709..84423371hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3822663
hg1922663
hg1822663
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv945n100
Supporting Variantsnssv3521268, nssv3706185, nssv3503575, nssv3511900, nssv3512519, nssv3706184, nssv3505099, nssv3520743, nssv3521340, nssv3505372
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)nsv1048978
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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