A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025308



Internal ID19114526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:102128569..102186521hg38UCSC Ensembl
Innerchr5:101464273..101522225hg19UCSC Ensembl
Innerchr5:101492172..101550124hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3857953
hg1957953
hg1857953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3748307, nssv3645890, nssv3645889
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)nsv1025308
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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