A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035022



Internal ID19124241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:96152197..96191092hg38UCSC Ensembl
Innerchr5:95487901..95526796hg19UCSC Ensembl
Innerchr5:95513657..95552552hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3838896
hg1938896
hg1838896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639941
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)nsv1035022
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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