A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997549



Internal ID18810399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:157241664..157392700hg38UCSC Ensembl
Innerchr1:157211454..157362490hg19UCSC Ensembl
Innerchr1:155478078..155629114hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38151037
hg19151037
hg18151037
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv441n100
Supporting Variantsnssv3704738
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)nsv997549
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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