A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009991



Internal ID19099210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:34625845..34648667hg38UCSC Ensembl
Innerchr1:35091446..35114268hg19UCSC Ensembl
Innerchr1:34864033..34886855hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3822823
hg1922823
hg1822823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv147n100
Supporting Variantsnssv3472637, nssv3470263
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)nsv1009991
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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