A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029655



Internal ID19118873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:85992440..86083720hg38UCSC Ensembl
Innerchr5:85288258..85379538hg19UCSC Ensembl
Innerchr5:85324014..85415294hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3891281
hg1991281
hg1891281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639176
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)nsv1029655
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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