A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034834



Internal ID19124055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:104361328..104446262hg38UCSC Ensembl
Innerchr5:103697029..103781963hg19UCSC Ensembl
Innerchr5:103724928..103809862hg18UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg3884935
hg1984935
hg1884935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5755n100
Supporting Variantsnssv3645982, nssv3746472, nssv3645986, nssv3645984, nssv3645985, nssv3645983
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)nsv1034834
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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