A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019525



Internal ID19108743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:24768269..24781707hg38UCSC Ensembl
Innerchr5:24768378..24781816hg19UCSC Ensembl
Innerchr5:24804135..24817573hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3813439
hg1913439
hg1813439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635950
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)nsv1019525
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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