A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029698



Internal ID19118917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:50716059..50951075hg38UCSC Ensembl
Innerchr8:51628619..51863635hg19UCSC Ensembl
Innerchr8:51791172..52026188hg18UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38235017
hg19235017
hg18235017
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7213n100
Supporting Variantsnssv3687478
Samples
Known GenesSNTG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029698
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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