A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022404



Internal ID19111622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9902717..9922281hg38UCSC Ensembl
Innerchr5:9902829..9922393hg19UCSC Ensembl
Innerchr5:9955829..9975393hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3819565
hg1919565
hg1819565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5567n100
Supporting Variantsnssv3638189
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)nsv1022404
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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