A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021146



Internal ID19110364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:150815610..150853799hg38UCSC Ensembl
Innerchr5:150195172..150233361hg19UCSC Ensembl
Innerchr5:150175365..150213554hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3838190
hg1938190
hg1838190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648173
Samples
Known GenesIRGM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021146
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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