A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021415



Internal ID19110632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8704114..8747030hg38UCSC Ensembl
Innerchr5:8704226..8747142hg19UCSC Ensembl
Innerchr5:8757226..8800142hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3842917
hg1942917
hg1842917
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5564n100
Supporting Variantsnssv3746430, nssv3746431
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)nsv1021415
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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