A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005999



Internal ID19095217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:92716216..92833236hg38UCSC Ensembl
Innerchr4:93637367..93754387hg19UCSC Ensembl
Innerchr4:93856390..93973410hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38117021
hg19117021
hg18117021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3742892
Samples
Known GenesGRID2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005999
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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