A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019760



Internal ID19108978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:50716059..50949590hg38UCSC Ensembl
Innerchr8:51628619..51862150hg19UCSC Ensembl
Innerchr8:51791172..52024703hg18UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38233532
hg19233532
hg18233532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7213n100
Supporting Variantsnssv3687477
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)nsv1019760
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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