A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998436



Internal ID19157972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:186202587..186237056hg38UCSC Ensembl
Innerchr1:186171719..186206188hg19UCSC Ensembl
Innerchr1:184438342..184472811hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3834470
hg1934470
hg1834470
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv481n100
Supporting Variantsnssv3499057
Samples
Known GenesMIR548F1, RNU6-72P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998436
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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