A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034130



Internal ID19123352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9901840..9922791hg38UCSC Ensembl
Innerchr5:9901952..9922903hg19UCSC Ensembl
Innerchr5:9954952..9975903hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3820952
hg1920952
hg1820952
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5567n100
Supporting Variantsnssv3638126, nssv3638125, nssv3638129, nssv3638124, nssv3638128, nssv3638131, nssv3638132, nssv3638123, nssv3638127, nssv3638130
Samples
Known GenesLOC285692
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034130
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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