A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007318



Internal ID19096537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:61618288..61647430hg38UCSC Ensembl
Innerchr1:62083960..62113102hg19UCSC Ensembl
Innerchr1:61856548..61885690hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3829143
hg1929143
hg1829143
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3475224
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)nsv1007318
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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