A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024075



Internal ID19113292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:101420320..101486554hg38UCSC Ensembl
Innerchr5:100756024..100822258hg19UCSC Ensembl
Innerchr5:100783923..100850157hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3866235
hg1966235
hg1866235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3645821
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)nsv1024075
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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