A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016924



Internal ID19106141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:116197368..116274323hg38UCSC Ensembl
Innerchr5:115533065..115610020hg19UCSC Ensembl
Innerchr5:115560964..115637919hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3876956
hg1976956
hg1876956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5791n100
Supporting Variantsnssv3647103, nssv3647100, nssv3647101, nssv3647102, nssv3746591, nssv3647104
Samples
Known GenesCOMMD10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016924
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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