A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009913



Internal ID19099132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:79075272..79151262hg38UCSC Ensembl
Innerchr1:79540957..79616947hg19UCSC Ensembl
Innerchr1:79313545..79389535hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3875991
hg1975991
hg1875991
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv202n100
Supporting Variantsnssv3468878
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)nsv1009913
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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