A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026906



Internal ID19116124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:99986588..100112652hg38UCSC Ensembl
Innerchr5:99322292..99448356hg19UCSC Ensembl
Innerchr5:99350191..99476255hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38126065
hg19126065
hg18126065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5733n100
Supporting Variantsnssv3645758
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)nsv1026906
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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