A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030830



Internal ID19120049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64683555..64930080hg38UCSC Ensembl
Innerchr9:69695973..69942498hg19UCSC Ensembl
Innerchr9:68985793..69232318hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38246526
hg19246526
hg18246526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7660n100
Supporting Variantsnssv3696163
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)nsv1030830
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer