A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007555



Internal ID19096774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:229674156..229691561hg38UCSC Ensembl
Innerchr1:229809903..229827308hg19UCSC Ensembl
Innerchr1:227876526..227893931hg18UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3817406
hg1917406
hg1817406
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3705523
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)nsv1007555
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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