A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022234



Internal ID18764768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:150152380..150188407hg38UCSC Ensembl
Innerchr5:149531943..149567970hg19UCSC Ensembl
Innerchr5:149512136..149548163hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3836028
hg1936028
hg1836028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648166
Samples
Known GenesCDX1, PDGFRB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022234
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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