A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021381



Internal ID19110598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:116174252..116232496hg38UCSC Ensembl
Innerchr5:115509949..115568193hg19UCSC Ensembl
Innerchr5:115537848..115596092hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3858245
hg1958245
hg1858245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3746590
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)nsv1021381
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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