A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034299



Internal ID19123521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64683555..64886202hg38UCSC Ensembl
Innerchr9:69695973..69898620hg19UCSC Ensembl
Innerchr9:68985793..69188440hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38202648
hg19202648
hg18202648
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7660n100
Supporting Variantsnssv3759741, nssv3696158
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)nsv1034299
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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