A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028930



Internal ID19118149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:92859065..93079405hg38UCSC Ensembl
Innerchr5:92194772..92415111hg19UCSC Ensembl
Innerchr5:92220528..92440867hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38220341
hg19220340
hg18220340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5716n100
Supporting Variantsnssv3639932
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)nsv1028930
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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