A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014866



Internal ID19104083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:55593381..55663419hg38UCSC Ensembl
Innerchr1:56059054..56129092hg19UCSC Ensembl
Innerchr1:55831642..55901680hg18UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3870039
hg1970039
hg1870039
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3478505
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)nsv1014866
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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