A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001572



Internal ID19090789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:87893138..87934812hg38UCSC Ensembl
Innerchr3:87942288..87983962hg19UCSC Ensembl
Innerchr3:88024978..88066652hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3841675
hg1941675
hg1841675
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596278
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)nsv1001572
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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