A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005599



Internal ID19094816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:113318902..113378267hg38UCSC Ensembl
Innerchr1:113861524..113920889hg19UCSC Ensembl
Innerchr1:113663047..113722412hg18UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3859366
hg1959366
hg1859366
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv292n100
Supporting Variantsnssv3702055
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)nsv1005599
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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