A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1040899



Internal ID15894085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:118856103..118906159hg38UCSC Ensembl
Innerchr5:118191798..118241854hg19UCSC Ensembl
Innerchr5:118219697..118269753hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3850057
hg1950057
hg1850057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599563
Supporting Variants
Samples
Known GenesDTWD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1040899
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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