A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997467



Internal ID19157003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:40881523..40922990hg38UCSC Ensembl
Innerchr1:41347195..41388662hg19UCSC Ensembl
Innerchr1:41119782..41161249hg18UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3841468
hg1941468
hg1841468
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv155n100
Supporting Variantsnssv3463729
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)nsv997467
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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