A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027747



Internal ID19116965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13294204..13356020hg38UCSC Ensembl
Innerchr7:13333829..13395645hg19UCSC Ensembl
Innerchr7:13300354..13362170hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3861817
hg1961817
hg1861817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643132
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)nsv1027747
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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