A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011229



Internal ID18753763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:31566071..31606805hg38UCSC Ensembl
Innerchr1:32031672..32072406hg19UCSC Ensembl
Innerchr1:31804259..31844993hg18UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg3840735
hg1940735
hg1840735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3472082
Samples
Known GenesTINAGL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011229
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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