A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030526



Internal ID19119745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29125695..29204079hg38UCSC Ensembl
Innerchr5:29125802..29204186hg19UCSC Ensembl
Innerchr5:29161559..29239943hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3878385
hg1978385
hg1878385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635995
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)nsv1030526
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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