A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020930



Internal ID19110148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:19015972..19279450hg38UCSC Ensembl
Innerchr5:19016081..19279559hg19UCSC Ensembl
Innerchr5:19051838..19315316hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38263479
hg19263479
hg18263479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5597n100
Supporting Variantsnssv3745828
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)nsv1020930
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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