A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999947



Internal ID19159483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:163773199..163836212hg38UCSC Ensembl
Innerchr1:163742436..163805449hg19UCSC Ensembl
Innerchr1:162009060..162072073hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3863014
hg1963014
hg1863014
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3482762
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)nsv999947
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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