A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032789



Internal ID19122011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:101549894..101606706hg38UCSC Ensembl
Innerchr5:100885598..100942410hg19UCSC Ensembl
Innerchr5:100913497..100970309hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3856813
hg1956813
hg1856813
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3645823
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)nsv1032789
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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