A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021568



Internal ID19110786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:142242319..142309792hg38UCSC Ensembl
Innerchr5:141621884..141689357hg19UCSC Ensembl
Innerchr5:141602068..141669541hg18UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3867474
hg1967474
hg1867474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3746645
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021568
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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