A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001046



Internal ID19090263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158491773..158533548hg38UCSC Ensembl
Innerchr1:158461563..158503338hg19UCSC Ensembl
Innerchr1:156728187..156769962hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3841776
hg1941776
hg1841776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3486121
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)nsv1001046
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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