A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024749



Internal ID19113966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:162977901..163035319hg38UCSC Ensembl
Innerchr5:162404907..162462325hg19UCSC Ensembl
Innerchr5:162337485..162394903hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3857419
hg1957419
hg1857419
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648233
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)nsv1024749
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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