A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037361



Internal ID19126580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82650973..82671549hg38UCSC Ensembl
Innerchr10:84410729..84431305hg19UCSC Ensembl
Innerchr10:84400709..84421285hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3820577
hg1920577
hg1820577
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv945n100
Supporting Variantsnssv3521486, nssv3510118, nssv3706173, nssv3516824, nssv3511380, nssv3506501, nssv3510500, nssv3503745, nssv3706172, nssv3706174, nssv3503852, nssv3706175, nssv3706171, nssv3518761, nssv3519615, nssv3706178, nssv3706176, nssv3706180, nssv3706177, nssv3706179, nssv3503926, nssv3518378, nssv3505545, nssv3511762
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)nsv1037361
Frequency
Sample Size11257
Observed Gain24
Observed Loss0
Observed Complex0
Frequencyn/a


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