A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026660



Internal ID19115878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:101607355..101911366hg38UCSC Ensembl
Innerchr5:100943059..101247070hg19UCSC Ensembl
Innerchr5:100970958..101274969hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38304012
hg19304012
hg18304012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5742n100
Supporting Variantsnssv3645826, nssv3645827
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)nsv1026660
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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