A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007154



Internal ID19096372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:76703898..76725852hg38UCSC Ensembl
Innerchr1:77169583..77191537hg19UCSC Ensembl
Innerchr1:76942171..76964125hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3821955
hg1921955
hg1821955
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv199n100
Supporting Variantsnssv3465461, nssv3477166, nssv3476914, nssv3466395, nssv3466622, nssv3471469, nssv3466461
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007154
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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