A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026670



Internal ID19115888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:11686597..11734614hg38UCSC Ensembl
Innerchr7:11726224..11774241hg19UCSC Ensembl
Innerchr7:11692749..11740766hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3848018
hg1948018
hg1848018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6267n100
Supporting Variantsnssv3642938
Samples
Known GenesTHSD7A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026670
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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