A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173102



Internal ID15878895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:108813740..108829252hg38UCSC Ensembl
Innerchr1:109356362..109371874hg19UCSC Ensembl
Innerchr1:109157885..109173397hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3815513
hg1915513
hg1815513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv547416
Supporting Variants
SamplesHGDP01275
Known GenesAKNAD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173102
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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