A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016099



Internal ID19105317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:182278531..182299044hg38UCSC Ensembl
Innerchr4:183199684..183220197hg19UCSC Ensembl
Innerchr4:183436678..183457191hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3820514
hg1920514
hg1820514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635601
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)nsv1016099
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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