A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026068



Internal ID19115285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:9589919..9647886hg38UCSC Ensembl
Innerchr7:9629549..9687516hg19UCSC Ensembl
Innerchr7:9596074..9654041hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3857968
hg1957968
hg1857968
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752877
Samples
Known GenesPER4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026068
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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