A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030798



Internal ID19120017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9898850..9922791hg38UCSC Ensembl
Innerchr5:9898962..9922903hg19UCSC Ensembl
Innerchr5:9951962..9975903hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3823942
hg1923942
hg1823942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5567n100
Supporting Variantsnssv3638109
Samples
Known GenesLOC285692
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030798
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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