A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029970



Internal ID19119189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:90644672..90691014hg38UCSC Ensembl
Innerchr5:89940489..89986831hg19UCSC Ensembl
Innerchr5:89976245..90022587hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3846343
hg1946343
hg1846343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5715n100
Supporting Variantsnssv3639187
Samples
Known GenesGPR98
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029970
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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