A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013226



Internal ID19102444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:59967404..60135273hg38UCSC Ensembl
Innerchr1:60433076..60600945hg19UCSC Ensembl
Innerchr1:60205664..60373533hg18UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38167870
hg19167870
hg18167870
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3474726
Samples
Known GenesC1orf87
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013226
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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