A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009230



Internal ID19098448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:83230703..83240797hg38UCSC Ensembl
Innerchr4:84151856..84161950hg19UCSC Ensembl
Innerchr4:84370880..84380974hg18UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3810095
hg1910095
hg1810095
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633900
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)nsv1009230
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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