A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033788



Internal ID19123009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:101892213..102042511hg38UCSC Ensembl
Innerchr5:101227917..101378215hg19UCSC Ensembl
Innerchr5:101255816..101406114hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38150299
hg19150299
hg18150299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3645884
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)nsv1033788
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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