A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021408



Internal ID19110625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:104361328..104453791hg38UCSC Ensembl
Innerchr5:103697029..103789492hg19UCSC Ensembl
Innerchr5:103724928..103817391hg18UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg3892464
hg1992464
hg1892464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5755n100
Supporting Variantsnssv3645987
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)nsv1021408
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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