A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015781



Internal ID19104999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:106778097..106811381hg38UCSC Ensembl
Innerchr5:106113798..106147082hg19UCSC Ensembl
Innerchr5:106141697..106174981hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3833285
hg1933285
hg1833285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5772n100
Supporting Variantsnssv3646938
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)nsv1015781
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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